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Books on the topic 'Chromosome polymorphism'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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1

Wyandt, Herman E., and Vijay S. Tonk. Human Chromosome Variation: Heteromorphism and Polymorphism. Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-0896-9.

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2

Wyandt, Herman E. Human Chromosome Variation: Heteromorphism and Polymorphism. Springer Science+Business Media B.V., 2012.

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3

Wyandt, Herman E., Golder N. Wilson, and Vijay S. Tonk. Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis. Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3035-2.

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4

universitet, Københavns, ed. Characterization of DNA polymorphisms on human chromosome 21 and their use in the study of unbalanced karyotypes, with special reference to nondisjunction in trisomy 21. Alma, 1996.

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5

Krimbas, Costas B. Drosophila subobscura: Biology, genetics, and inversion polymorphism. Kovač, 1993.

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6

University), National Seminar on Cytopolymorphism in Plants (1989 Annamalai. Proceedings of the National Seminar on Cytopolymorphism in Plants, 25th-27th February 1989. Annamalai University, 1991.

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7

R, Taylor G., ed. Laboratory methods for the detection of mutations and polymorphisms in DNA. CRC Press, 1997.

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8

Ellegren, Hans. Genome analysis with microsatellite markers. Dept. of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, 1993.

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9

1956-, Kwok Pui-Yan, ed. Single nucleotide polymorphisms: Methods and protocols. Humana Press, 2003.

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10

Amster, Guy. Life history effects on neutral polymorphism and divergence rates, in autosomes and sex chromosomes. [publisher not identified], 2019.

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11

Westphal, Eva-Maria. Restriktionsfragment-Längen-Polymorphismen im Bereich des Tyrosinaminotransferase-Gens als Marker für Tyrosinämie Typ II und bei der Kartierung verschiedener Loci auf Chromosom 16 q. [s.n.], 1987.

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12

Atlas of human chromosome heteromorphisms. Kluwer Academic·, 2002.

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13

Drosophila inversion polymorphism. CRC Press, 1992.

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14

Wilson, Golder N., Herman E. Wyandt, and Vijay S. Tonk. Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis. Springer, 2017.

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15

Wilson, Golder N., Herman E. Wyandt, and Vijay S. Tonk. Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis. Springer, 2018.

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16

India, Anthropological Survey Of, and D. N. A. Polymorphism DNA Polymorphism Consortium. Genomic Diversity in People of India: Focus on MtDNA and y-Chromosome Polymorphism. Springer Singapore Pte. Limited, 2021.

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17

India, Anthropological Survey Of, and D. N. A. Polymorphism DNA Polymorphism Consortium. Genomic Diversity in People of India: Focus on MtDNA and y-Chromosome Polymorphism. Springer, 2022.

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18

Kwok, Pui-Yan. Single Nucleotide Polymorphisms: Methods and Protocols (Methods in Molecular Biology). Humana Press, 2002.

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19

Komar, Anton A. Single Nucleotide Polymorphisms: Methods and Protocols. Humana Press, 2012.

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20

Kwok, Pui-Yan. Single Nucleotide Polymorphisms: Methods and Protocols. Humana Press, 2003.

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21

Divan, Aysha, and Janice A. Royds. 2. DNA. Oxford University Press, 2016. http://dx.doi.org/10.1093/actrade/9780198723882.003.0002.

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Another significant milestone was the publication in 2003 of the complete sequence of the human genome—the entire DNA contained within the forty-six chromosomes located in the nucleus of each human somatic (body) cell. Once this was published, further worldwide projects were launched to work out what the functions of these genes and other regions of the genome actually were. ‘DNA’ outlines the components of the human genome and their organization; DNA replication; mutations and correction mechanisms; polymorphisms; and new DNA technologies, including gene cloning, the polymerase chain reaction
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22

Weihbrecht, Sebastian Bernd. Assoziationen zwischen Polymorphismen im ˜Topoisomerase-II-α-Gen œ[Topoisomerase-II-alpha-Gen] mit der Länge des HER2-Amplikons suf Chromosom 17: Implikationen für Mechanismen der Genamplifikation und die Prognose bei Mammkarzinompatientinnen. 2010.

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23

Vermeulen, Roel, Douglas A. Bell, Dean P. Jones, et al. Application of Biomarkers in Cancer Epidemiology. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190238667.003.0006.

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Advancements in OMICs are now enabling investigators to explore comprehensively the biological consequences of exogenous and endogenous exposures by detecting molecular signatures of exposure, early signs of adverse biological effects, preclinical disease, and molecularly defined cancer subtypes. These new technologies have proven invaluable for assembling a comprehensive portrait of human exposure, health, and disease. This includes hypothesis-driven biomarkers, as well as platforms that can agnostically analyze entire biologic processes and “compartments,” including the measurement of small
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24

Weihbrecht, Sebastian Bernd. Assoziationen zwischen Polymorphismen im ˜Topoisomerase-II-α-Gen œ[Topoisomerase-II-alpha-Gen] mit der Länge des HER2-Amplikons auf Chromosom 17: Implikationen für Mechanismen der Genamplifikation und die Prognose bei Mammakarzinompatientinnen. 2010.

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25

Samuels, Jack, Marco A. Grados, Elizabeth Planalp, and O. Joseph Bienvenu. Genetic Understanding of OCD and Spectrum Disorders. Edited by Gail Steketee. Oxford University Press, 2012. http://dx.doi.org/10.1093/oxfordhb/9780195376210.013.0025.

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This chapter reviews the evidence for the genetic etiology of OCD and spectrum conditions. A genetic basis is supported by the familial aggregation of OCD; evidence for involvement of genes of major effect in segregation analyses; and higher concordance for OCD in identical than non-identical twins. Recent studies also support linkage of OCD to specific chromosomal regions and association of OCD with specific genetic polymorphisms. However, specific genes causing OCD have not yet been firmly established. The search for genes is complicated by the clinical and etiologic heterogeneity of OCD, as
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26

König, Ulrich. Untersuchung chromosomaler Polymorphismen bei Familien mit Kindern mit einer freien Trisomie 21 unter besonderer Berücksichtigung der Herkunft des überzähligen Chromosoms 21. 1990.

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27

Rabinow, Paul. French DNA: Trouble in Purgatory. University Of Chicago Press, 2002.

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28

Rabinow, Paul. French DNA: Trouble in Purgatory. University Of Chicago Press, 1999.

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