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Relevant bibliographies by topics / Phenotype variability

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Academic literature on the topic 'Phenotype variability'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 February 2022

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Journal articles on the topic "Phenotype variability"

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Ayroles, Julien F., Sean M. Buchanan, Chelsea O’Leary, et al. "Behavioral idiosyncrasy reveals genetic control of phenotypic variability." Proceedings of the National Academy of Sciences 112, no. 21 (2015): 6706–11. http://dx.doi.org/10.1073/pnas.1503830112.

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Quantitative genetics has primarily focused on describing genetic effects on trait means and largely ignored the effect of alternative alleles on trait variability, potentially missing an important axis of genetic variation contributing to phenotypic differences among individuals. To study the genetic effects on individual-to-individual phenotypic variability (or intragenotypic variability), we used Drosophila inbred lines and measured the spontaneous locomotor behavior of flies walking individually in Y-shaped mazes, focusing on variability in locomotor handedness, an assay optimized to measu

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von Both, Ulrich, Anna Buerckstuemmer, Kirsten Fluegge, and Reinhard Berner. "Heterogeneity of Genotype-Phenotype Correlation among Macrolide-Resistant Streptococcus agalactiae Isolates." Antimicrobial Agents and Chemotherapy 49, no. 7 (2005): 3080–82. http://dx.doi.org/10.1128/aac.49.7.3080-3082.2005.

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ABSTRACT Seventy-four erythromycin-resistant group B Streptococcus isolates were analyzed regarding their phenotype-genotype and phenotype-serotype correlation. Four different phenotypes were assessed, one of them for the first time. ermB and ermTR were the most frequent genotypes (80%). The most prevalent serotype III showed great phenotypic variability while serotype V was strongly associated only with two different phenotypes.

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Moser, Lukas, Silvan Hess, Henrik Behrend, and Michael Hirschmann. "Variability of functional knee phenotypes in osteoarthritic knees shows that a more personalized approach in TKA is needed." Orthopaedic Journal of Sports Medicine 8, no. 5_suppl4 (2020): 2325967120S0030. http://dx.doi.org/10.1177/2325967120s00300.

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Aims and Objectives: Recently, the functional knee phenotype concept was introduced as a new system to classify the coronal alignment of the lower limb. Until now, this concept has only been applied to non-osteoarthritic knees. The purpose of this study was therefore to phenotype osteoarthritic knees according to this concept and investigate the distribution of these phenotypes. Materials and Methods: Preoperative CT scans of osteoarthritic knees scheduled for TKA collected between January 2017 and December 2019 in the KneePLAN 3D database (Symbios Orthopédie S.A.) were reviewed for patients m

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Park, J., A. Brureau, K. Kernan, et al. "Inputs drive cell phenotype variability." Genome Research 24, no. 6 (2014): 930–41. http://dx.doi.org/10.1101/gr.161802.113.

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Volo, T., C. Morando, E. Leonardi, et al. "A028 Unraveling DFNB1 phenotype variability." International Journal of Pediatric Otorhinolaryngology 75 (May 2011): 6. http://dx.doi.org/10.1016/s0165-5876(11)70029-5.

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Gilbert, James R., James J. Cray, Amy Kreithen, et al. "Genetic Homozygosity and Phenotypic Variability in Craniosynostotic Rabbits." Cleft Palate-Craniofacial Journal 54, no. 1 (2017): 94–99. http://dx.doi.org/10.1597/15-226.

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Background Craniosynostosis ranges in severity from single suture involvement with prenatal onset to multiple suture involvement with postnatal onset. The present study was designed to test the hypothesis that increasing homozygosity may be responsible for more severe phenotypic expression by examining the relationship between inbreeding and phenotypic expression in synostotic rabbits. Methods Data were obtained from 173 litters and 209 rabbits with familial craniosynostosis. Five distinct phenotypes were identified (normal n = 62; unicoronal delayed onset synostosis (DOS) n = 47; bicoronal DO

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Schirwani, Schaida, Kay Metcalfe, Bart Wagner, Ian Berry, Glenda Sobey, and Rosalyn Jewell. "DSE associated musculocontractural EDS, a milder phenotype or phenotypic variability." European Journal of Medical Genetics 63, no. 4 (2020): 103798. http://dx.doi.org/10.1016/j.ejmg.2019.103798.

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Regev, Miriam, Ben Pode-Shakked, Jeffrey M. Jacobson, Annick Raas-Rothschild, David B. Goldstein, and Yair Anikster. "Phenotype variability in Hajdu-Cheney syndrome." European Journal of Medical Genetics 62, no. 1 (2019): 35–38. http://dx.doi.org/10.1016/j.ejmg.2018.04.015.

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Ong, M. T., J. Willoughby, D. Connolly, A. Fadilah, S. R. Mordekar, and D. S. Johnson. "Genotype-phenotype variability of DARS mutations." European Journal of Paediatric Neurology 21 (June 2017): e58. http://dx.doi.org/10.1016/j.ejpn.2017.04.914.

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Mu, Weiyi, Teresa Heller, and Kristin W. Barañano. "Two siblings with a novel variant of EXOSC3 extended phenotypic spectrum of pontocerebellar hypoplasia 1B to an exceptionally mild form." BMJ Case Reports 14, no. 1 (2021): e236732. http://dx.doi.org/10.1136/bcr-2020-236732.

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Pontocerebellar hypoplasia type 1B (PCH1B) describes an autosomal recessive neurological condition that involves hypoplasia or atrophy of the cerebellum and pons, resulting in neurocognitive impairments. Although there is phenotypic variability, this is often an infantile lethal condition, and most cases have been described to be congenital and neurodegenerative. PCH1B is caused by mutations in the gene EXOSC3, which encodes exosome component 3, a subunit of the human RNA exosome complex. A range of pathogenic variants with some correlation to phenotype have been reported. The most commonly re

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Dissertations / Theses on the topic "Phenotype variability"

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Penwill, Lynsey Ann. "Phenotype variability determination using Airy Disc analysis." Thesis, University of Exeter, 2013. http://hdl.handle.net/10871/15717.

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Rapid phenotype identification and screening is a relatively unexplored field compared with genotype screening probably owing to a lack of appropriate technology. The Lensless microscope has a large field of view and allows the capture of the diffraction pattern from a large number of cells simultaneously, its potential to screen growth phenotypes will be evaluated in this thesis. A simple algorithm has been developed to measure intensity changes in the Airy Disc First Fringe (ADFF) from which length and width dimensions can be derived from scattering objects with an accuracy of 5%, except for

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Taggart, Emma Louise. "Variability of the alagille syndrome phenotype : assessment of molecular mechanisms." Thesis, King's College London (University of London), 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.419885.

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Smith, Shad Benjamin. "Positional cloning of genes contributing to variability in nociceptive and analgesic phenotypes." Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=103009.

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Variability between individuals in pain and analgesia phenotypes is often observed in both clinical and experimental settings. The source of this variability has long been attributed to the interplay of environmental and genetic factors, but we have only recently begun identifying these determinants. Experiments comparing isogenic strains of mice have suggested that different pain tests may share a genetic basis; likewise, analgesic magnitude induced by disparate drug classes may be influenced by a common set of genes.<br>We have presently used a quantitative trait locus mapping strategy to se

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Aissat, Abdelrazak. "Variabilité phénotypique et épissage : combinaison d'analyses in vitro et in silico du gène CFTR." Thesis, Paris Est, 2012. http://www.theses.fr/2012PEST0060.

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Depuis plusieurs décennies, l’étude des conséquences des mutations pathogéniques a permisnon seulement de définir l’origine de nombreuses maladies génétiques humaines, héréditaires ou non,mais également de contribuer à l’interprétation de la variabilité phénotypique inter-individus au seind’une pathologie donnée. Les mutations induisant une perte de fonction de la protéine synthétisée ouune protéine incomplète ont été et sont encore les plus étudiées. Avec l’introduction des technologiesde séquençage à haut-débit, le nombre de variants faux-sens, silencieux ou introniques détectés auniveau des

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Marsom, Fernando Augusto de Lima. "Análise de genes modificadores relacionados à gravidade clínica da fibrose cística." [s.n.], 2011. http://repositorio.unicamp.br/jspui/handle/REPOSIP/308362.

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Orientador: Antonio Fernando Ribeiro<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas<br>Made available in DSpace on 2018-08-19T10:15:56Z (GMT). No. of bitstreams: 1 Marsom_FernandoAugustodeLima_M.pdf: 12182231 bytes, checksum: e98655cb1347b5ba1ffbceac13daebb0 (MD5) Previous issue date: 2011<br>Resumo: Introdução: A fibrose cística (FC) se manifesta clinicamente com várias formas de gravidade, moduladas por diferentes genótipos e o meio ambiente. Enquanto as classes das mutações no gene CFTR ("Cystic Fibrosis Transmembrane Conductance Regulator") e

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Eddins, Amy C. "The Influence of Local Forage Variability on White-tailed Deer (Odocoileus virginianus) Body Size at Fort Hood, Texas." Thesis, University of North Texas, 2015. https://digital.library.unt.edu/ark:/67531/metadc822844/.

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Nutritional quality and availability is thought to regulate geographic patterns of variability in animal body size due to phenotypic plasticity. The purpose of this study is to determine how vegetation quality, abundance and population density influence white-tailed deer (Odocoileus virginianus) body size on a subregional spatial scale at Fort Hood, Texas. Harvest and census records are used to test the hypothesis that white-tailed deer exhibit phenotypic plasticity (e.g. larger body size) in response to differences in vegetation quality and availability. Results from these analyses suggest

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Fabrèges, Dimitri. "Phenotypic Variations In Animal Morphogenesis : Sea Urchin Twins And Cloned Rabbits." Thesis, Université Paris-Saclay (ComUE), 2016. http://www.theses.fr/2016SACLS010/document.

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La variabilité est une propriété intrinsèque aux systèmes biologiques, essentielle pour l'évolution et l'embryogénèse. Souvent considérée comme du bruit, ce n'est que récemment que l'aléatoire des processus biologiques a commencé à être systématiquement étudié. Cette thèse pose les questions suivantes : qu'est-ce qu'un développement normal ? Quel est l'étendue et le rôle de la variabilité dans la robustesse et la résilience du développement embryonnaire ?Ces questions sont posées pour le lapin (Oryctolagus cuniculus) et l'oursin (Paracentrotus lividus et Sphaerechinus granularis).Nous nous som

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Chaoui, Asma. "Bases moléculaires et cellulaires du syndrome de Waardenburg : de la génétique à la fonction de SOX10." Thesis, Paris Est, 2013. http://www.theses.fr/2013PEST0103.

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Burge, J. A. "Mechanisms of phenotypic variability in Myotonia Congenita." Thesis, University College London (University of London), 2013. http://discovery.ucl.ac.uk/1401157/.

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The severity of Myotonia Congenita varies not only across individuals with different CLCN1 genotypes, but also within a pedigree, and can even fluctuate over time within a single individual in response to environmental circumstances. The functional consequences of eight naturally occurring sequence variants in the skeletal muscle chloride channel gene, CLCN1, were examined by whole cell patch-clamp of HEK293T cells expressing the gene product, ClC-1, in order to investigate potential differences in their mechanisms of pathogenicity. G276D and G523D caused complete loss of function, while S289G

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Crotti, Pablo. "Phenotypic variability, cell size and population fitness." Thesis, Imperial College London, 2015. http://hdl.handle.net/10044/1/43964.

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In all biological systems, phenotypes are quantitative measures of an organism's traits. To understand the relation between a genotype and phenotypes, the influence of genetic perturbations, such as gene deletions, on phenotypes is studied. Although it is common practice to look at the mean value of phenotypes to detect changes, it is less common to model such modifications by considering phenotypic variability. However, phenotypic variability could also contain important information about the phenotype-genotype map. Also, phenotypic variability is a determinant of an organism's robustness and

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Books on the topic "Phenotype variability"

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Bergmann, Carsten, and Klaus Zerres. Autosomal recessive polycystic kidney disease. Edited by Neil Turner. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0313.

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Autosomal recessive polycystic kidney disease (ARPKD) is an important cause of childhood renal- and liver-related morbidity and mortality with variable disease expression. Many patients manifest peri- or neonatally with a mortality rate of 30–50%, whereas others survive to adulthood with only minor clinical features. ARPKD is typically caused by mutations in the PKHD1 gene that encodes a 4074-amino acid type 1 single-pass transmembrane protein called fibrocystin or polyductin. Fibrocystin/polyductin is among other cystoproteins expressed in primary cilia, basal bodies, and centrosomes, but its

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Williams, Karen D., and Marla B. Sokolowski. Phenotypic plasticity. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198797500.003.0005.

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Why is there so much variation in insect behavior? This chapter will address the sources of behavioral variability, with a particular focus on phenotypic plasticity. Variation in social, nutritional, and seasonal environmental contexts during development and adulthood can give rise to phenotypic plasticity. To delve into mechanism underlying behavioral flexibility in insects, examples of polyphenisms, a type of phenotypic plasticity, will be discussed. Selected examples reveal that environmental change can affect gene expression, which in turn can affect behavioral plasticity. These changes in

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Fabbri, Chiara, and Alessandro Serretti. The treatment of bipolar disorder in the era of personalized medicine: myth or promise? Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198748625.003.0031.

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Bipolar disorder (BD) is a chronic disease associated with high personal and socio-economic burden. Genetics accounts for 20–95% of variability in central nervous system drug disposition and pharmacodynamics, thus genetic markers are considered a promising way to develop tailored treatments and improve the prognosis of the disease. Among mood stabilizers, lithium response was the most investigated phenotype and the most replicated genes are involved in synaptic plasticity (BDNF), serotonergic (SLC6A4) and dopaminergic (DRD1) neurotransmission, and second messenger cascades (GSK3B). Relevant ph

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Neri, Giovanni, Luigi Boccuto, and Roger E. Stevenson, eds. Overgrowth Syndromes. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780190944896.001.0001.

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This book provides comprehensive details on a number of well-defined genetic disorders and a selection of less well-defined entities that include somatic overgrowth as a major manifestation. In addition to overgrowth, these syndromes each have their own distinguishing characteristics that benefit the clinician in making a specific diagnosis. In most cases, the causative genes are known, giving a means of laboratory confirmation of the diagnoses. A major distinction from other hereditary syndromes is a predisposition of patients with the overgrowth syndromes to develop neoplasms during childhoo

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Geri, Guillaume, and Jean-Paul Mira. Host–pathogen interactions in the critically ill. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0306.

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Infection by a pathogenic micro-organism triggers a coordinated activation of both innate and adaptive immune responses. The innate immune response quickly triggers an antimicrobial response that will initiate development of a pathogen-specific, long-lasting adaptive immune response. Accurate recognition of microbial-associated molecular patterns by pattern-recognition receptors (PRRs) is the cornerstone of this immediate response. Most studied PRRs are Toll-like receptors (TLRs) and their kinase signalling cascades that activate nuclear transcription factors, and induce gene expression and cy

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Jaffer, Amina, Anant Patel, and John Hurst. Chronic obstructive pulmonary disease. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199657742.003.0006.

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This chapter discusses the case of a 70-year-old man with his first presentation of chronic obstructive pulmonary disease. This case is used as a basis to explore and describe the diagnosis, investigation, and management of this condition. The chapter includes the evidence base and relative guidelines that support current practice, as well as highlighting useful learning points and providing expert opinion. The role of lung volume reduction surgery is discussed, and its potential benefits in selected patients highlighted. Phenotypic variability within chronic obstructive pulmonary disease is i

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Franco, Brunella. Oral-facial-digital type 1 syndrome. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0319_update_001.

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This chapter discusses oral-facial-digital type 1 syndrome (OFD1), which represents a rare syndromic form of inherited renal cystic disease associated with dysfunction of primary cilia. The disease is transmitted as an X-linked dominant male lethal trait. Embryonic lethality in affected hemizygous males is usually reported in the first and second trimesters of pregnancy. The clinical spectrum for this disease includes malformation of the face, oral cavity, and digits with a high degree of phenotypic variability, even within the same family, possibly due to X-inactivation. Renal cystic disease

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Vester, Udo, and Stefanie Weber. Renal coloboma syndrome. Edited by Adrian Woolf. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0360.

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Renal coloboma syndrome is characterized by hypodysplasia of the kidneys and optic never anomalies. Dominant mutations in the paired box PAX2 gene have been defined as the underlying cause. Paired box proteins are important proteins involved in early organogenesis and PAX2 is highly expressed in the kidney, eye, and ear. This pattern of expression explains the spectrum of anomalies observed in RCS patients. The phenotypic variability of mutation carriers is high but ocular anomalies are detectable in almost all affected individuals. In some patients hearing impairment is observed. End-stage re

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Stanghellini, Giovanni. Position-taking. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198792062.003.0037.

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This chapter argues that the extreme variability of schizophrenic phenotypes is a paradigmatic case study for explicating the dialectics between uncanny feelings of depersonalization/derealization and the attitude of the person who experiences them. Why do persons who suffer from these kinds of anomalous self-, body-, and world-experiences develop either a delusional form of schizophrenia or a ‘pauci-symptomatic’ type of this illness, or a schizotypal personality disorder? Why do delusions in people with schizophrenia take on so many different themes, and not only ontological ones, but also, f

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Book chapters on the topic "Phenotype variability"

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Loglisci, Corrado, Bachir Balech, and Donato Malerba. "Discovering Variability Patterns for Change Detection in Complex Phenotype Data." In Lecture Notes in Computer Science. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-25252-0_2.

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Smith, David W. E. "Variability in Life Span Functional Capacity." In Phenotypic Variation in Populations. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5460-4_18.

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Elston, Robert C. "The Use of Polymorphic Markers to Detect Genetic Variability." In Phenotypic Variation in Populations. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5460-4_11.

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Corey, Linda A., Lindon J. Eaves, and Walter E. Nance. "Variability in Anthropometric Traits in Twins and Their Families." In Phenotypic Variation in Populations. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5460-4_9.

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Schaie, K. Warner. "Variability in Cognitive Function in the Elderly: Implications for Societal Participation." In Phenotypic Variation in Populations. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5460-4_20.

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Mandel, Hanna, and Stanley H. Korman. "Phenotypic Variability (Heterogeneity) of Peroxisomal Disorders." In Advances in Experimental Medicine and Biology. Springer US, 2003. http://dx.doi.org/10.1007/978-1-4419-9072-3_2.

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Miller, Robert W. "Epidemiologic Evidence for Genetic Variability in the Frequency of Cancer: Ethnic Differences." In Phenotypic Variation in Populations. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5460-4_7.

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Kolonel, Laurence N. "Variability in Diet and its Relation to Risk in Ethnic and Migrant Groups." In Phenotypic Variation in Populations. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5460-4_14.

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Lecavalier, Luc. "Phenotypic Variability in Autism Spectrum Disorder: Clinical Considerations." In Handbook of Autism and Anxiety. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-06796-4_2.

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Mad’ari, Aladár, Petr Novak, and Norbert Žilka. "Phenotypic Variability and Clinical Staging of Canine Dementia." In Canine and Feline Dementia. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-53219-6_3.

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Conference papers on the topic "Phenotype variability"

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Ducharme, Francine M., Kate Thompson, Jpnathan Morin, G. Michael Davis, Joanie Gingras, and Francisco J. Noya. "High Physician Adherence To Phenotype-Specific Asthma Recommendations But Large Variability In Phenotype Recognition In Children." In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a5465.

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Marten, S., R. Knöfler, K. Trautmann, and O. Tiebel. "Laboratory phenotype variability in genetically proven von Willebrand disease type 2B." In 65th Annual Meeting of the Society of Thrombosis and Haemostasis Research. Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/s-0041-1728214.

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Boeckelmann, D., H. Glonnegger, F. Sobotta, et al. "Next-generation sequencing identified different types of Hermansky-Pudlak syndrome associated with phenotype variability." In 65th Annual Meeting of the Society of Thrombosis and Haemostasis Research. Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/s-0041-1728107.

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Bartolak-Suki, E., and B. Suki. "Variability in Stretch Amplitude Regulates Vascular Smooth Muscle Cell Phenotype: Implications for Pulmonary Arterial Hypertension." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a5052.

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Hill, Seamus, and Colm O'Riordan. "Examining the use of a non-trivial fixed genotype-phenotype mapping in genetic algorithms to induce phenotypic variability over deceptive uncertain landscapes." In 2011 IEEE Congress on Evolutionary Computation (CEC). IEEE, 2011. http://dx.doi.org/10.1109/cec.2011.5949780.

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Liovic, Petar, Ilija D. Šutalo, Laurence Meagher, and George O. Lovrecz. "Computations of Flow Environments in Medium-Scale Stirred-Tank Bioreactors for Stem Cell Expansion." In ASME 2014 4th Joint US-European Fluids Engineering Division Summer Meeting collocated with the ASME 2014 12th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/fedsm2014-21967.

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The flow in a New Brunswick Scientific (NBS (now Eppendorf)) 5 L stirred-tank bioreactor (STR) partially filled with 2.2 L of water and agitated at 60 rpm using a pitched-blade impeller is studied in this work, to determine the suitability of the configuration for expanding stem cell lines. Computational Fluid Dynamics (CFD) model development and testing in this work has found Large Eddy Simulation (LES) to be essential for model fidelity and for capturing spatiotemporal stress fluctuations. Stresses were at levels similar to or even higher than those known to damage stem cells or modulate the

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Long, David S., Hui Zhu, and Morton H. Friedman. "Quantifying the Motion of Murine Epicardial Coronary Arteries." In ASME 2008 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2008. http://dx.doi.org/10.1115/sbc2008-192065.

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Coronary artery atherosclerosis is a leading cause of morbidity and mortality in western societies. Atherosclerosis is a progressive fibroinflammatory disease identified by intimal thickening, the focal accumulation of lipids, fibrous elements, and cellular elements within the walls of large arteries. These lesions preferentially develop at arterial branches, the outer walls of bifurcations, and the inner walls of curved sections; the cause of this focal vasculopathy is not fully understood. It is, however, understood from epidemiological and clinical studies that individual susceptibility to

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Henderson, Charles M. "MORPHOLOGIC VARIABILITY OF SWEETOGNATHIDS: PHENOTYPIC OR GENOTYPIC?" In GSA Annual Meeting in Phoenix, Arizona, USA - 2019. Geological Society of America, 2019. http://dx.doi.org/10.1130/abs/2019am-341190.

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Markov, Nikita, Konstantin Ushenin, Yakov Bozhko, Mikhail Arkhipov, and Olga Solovyova. "Heart Rate Variability Reveals Two Phenotypes of Atrial Fibrillation." In 2021 IEEE Ural-Siberian Conference on Computational Technologies in Cognitive Science, Genomics and Biomedicine (CSGB). IEEE, 2021. http://dx.doi.org/10.1109/csgb53040.2021.9496013.

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Oksel, Ceyda, Raquel Granell, John Henderson, and Adnan Custovic. "Potential causes of variability in latent phenotypes of childhood wheeze." In ERS International Congress 2018 abstracts. European Respiratory Society, 2018. http://dx.doi.org/10.1183/13993003.congress-2018.pa1302.

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Reports on the topic "Phenotype variability"

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Friedman, Jan M. Analysis of Phenotypic Variability in Neurofibromatosis, Type 1. Defense Technical Information Center, 1998. http://dx.doi.org/10.21236/ada361846.

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Friedman, Jan M. Analysis of Phenotypic Variability in Neurofibromatosis, Type 1. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada392317.

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Friedman, Jan M. Analysis of Phenotypic Variability in Neurofibromatosis Type I (NF1). Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada403609.

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