Auswahl der wissenschaftlichen Literatur zum Thema „Prental diagnosis“
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Zeitschriftenartikel zum Thema "Prental diagnosis":
Ville, Y. „Congenital CMV infection — prental diagnosis and prenatal care“. Journal of Clinical Virology 36 (Januar 2006): S5—S6. http://dx.doi.org/10.1016/s1386-6532(06)80709-2.
Megier, P., und A. Desroches. „Prental color Doppler diagnosis of placenta previa accreta“. Ultrasound in Obstetrics & Gynecology 4, Nr. 5 (01.09.1994): 437. http://dx.doi.org/10.1046/j.1469-0705.1994.04050437.x.
Root, Mariah C., und Kelsy L. Fisher. „Prenatal Sonographic Detection of Ebstein’s Anomaly“. Journal of Diagnostic Medical Sonography 33, Nr. 3 (04.02.2017): 225–30. http://dx.doi.org/10.1177/8756479317691237.
Fountain-Dommer, Robin R., Scott M. Bradley, Andrew M. Atz, Martha R. Stroud, Geoffrey A. Forbus und Girish S. Shirali. „Outcome following, and impact of, prenatal identification of the candidates for the Norwood procedure“. Cardiology in the Young 14, Nr. 1 (Februar 2004): 32–38. http://dx.doi.org/10.1017/s1047951104001064.
Lazow, Stefanie P., Danielle M. Richman, Beatrice Dionigi, Steven J. Staffa, Carol B. Benson und Terry L. Buchmiller. „Prenatal Imaging Diagnosis of Suprarenal Lesions“. Fetal Diagnosis and Therapy 48, Nr. 3 (2021): 235–42. http://dx.doi.org/10.1159/000512689.
Gorla, Sudheer R., Abhishek Chakraborty, Ashish Garg, Rubee A. Gugol, Richard E. Kardon und Sethuraman Swaminathan. „Emerging trends in the prenatal diagnosis of complex CHD and its influence on infant mortality in this cohort“. Cardiology in the Young 29, Nr. 3 (26.12.2018): 270–76. http://dx.doi.org/10.1017/s1047951118002147.
Kang, Jiun. „The Promise of Whole-exome Sequencing for Prenatal Genetic Diagnosis“. Current Pharmacogenomics and Personalized Medicine 17, Nr. 1 (28.04.2020): 25–31. http://dx.doi.org/10.2174/1875692117666191106105918.
Bratt, Ewa-Lena, Stina Järvholm, Britt-Marie Ekman-Joelsson, Antje Johannsmeyer, Sven-Åke Carlsson, Lars-Åke Mattsson und Mats Mellander. „Parental reactions, distress, and sense of coherence after prenatal versus postnatal diagnosis of complex congenital heart disease“. Cardiology in the Young 29, Nr. 11 (16.09.2019): 1328–34. http://dx.doi.org/10.1017/s1047951119001781.
Khatib, Ghanim. „Prenatal Diagnosis of Congenital Mesoblastic Nephroma“. Perinatal Journal 21, Nr. 2 (01.08.2013): 85–88. http://dx.doi.org/10.2399/prn.13.0212007.
Dasari, Papa, und Pratima Aggrawal. „Prenatal diagnosis of congenital fetal malformations medically terminated: a retrospective analysis“. New Indian Journal of OBGYN 8, Nr. 1 (Juli 2021): 62–68. http://dx.doi.org/10.21276/obgyn.2021.8.1.13.
Dissertationen zum Thema "Prental diagnosis":
Marangoni, Martina. „Implementation of clinical exome sequencing in prenatal setting: comparing between prospective and retrospective cohort studies“. Doctoral thesis, Universite Libre de Bruxelles, 2021. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/331254.
Doctorat en Sciences biomédicales et pharmaceutiques (Médecine)
info:eu-repo/semantics/nonPublished
Leung, Kwok-yin, und 梁國賢. „Prenatal ultrasound prediction of homozygous α⁰-thalassemia“. Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hub.hku.hk/bib/B47454039.
published_or_final_version
Obstetrics and Gynaecology
Master
Doctor of Medicine
Overton, Timothy Graeme. „Minimally invasive prenatal diagnosis“. Thesis, Imperial College London, 2000. http://hdl.handle.net/10044/1/7869.
Crang-Svalenius, Elizabeth. „The use of routine ultrasound in pregnancy with special reference to normal and abnormal foetal growth, information and informed choice and the womens' experiences of the prenatal diagnostic aspects /“. Lund : Lund University, Dept. of Obstetrics and Gynaecology, University Hospital, 1997. http://catalog.hathitrust.org/api/volumes/oclc/39072830.html.
Miller, Chloe Louise. „A comparison of attitudes towards prenatal diagnosis and pre-implantation genetic diagnosis“. Thesis, University of Leeds, 2010. http://etheses.whiterose.ac.uk/1083/.
Lee, Sansan. „Genetic counseling perspectives on prenatal array CGH testing“. Waltham, Mass. : Brandeis University, 2009. http://dcoll.brandeis.edu/handle/10192/23259.
PULICANI, REISS BRIGITTE. „Diagnostic prenatal et ethique medicale“. Aix-Marseille 2, 1989. http://www.theses.fr/1989AIX20138.
LaPan, Amy C. „Prenatal testing, birth outcomes, and views of social workers“. online access from Digital Dissertation Consortium, 2005. http://libweb.cityu.edu.hk/cgi-bin/er/db/ddcdiss.pl?3202790.
Leung, Wing-cheong, und 梁永昌. „Rapid aneuploidy testing or traditional karyotyping, or both, in prenatal diagnosis“. Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2010. http://hub.hku.hk/bib/B4520553X.
Tedgård, Ulf. „Prenatal diagnosis of haemophilia psychological, social and ethical aspects /“. Malmö : Dept. of Pediatrics, University Hospital of Malmö, University of Lund, 1999. http://catalog.hathitrust.org/api/volumes/oclc/57455671.html.
Bücher zum Thema "Prental diagnosis":
Hahn, Sinuhe, und Laird G. Jackson, Hrsg. Prenatal Diagnosis. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-066-9.
Levy, Brynn, Hrsg. Prenatal Diagnosis. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-8889-1.
Abramsky, Lenore, und Jean Chapple, Hrsg. Prenatal Diagnosis. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-3027-9.
Weaver, David D. Catalog of prenatally diagnosed conditions. 2. Aufl. Baltimore: Johns Hopkins University Press, 1992.
Weaver, David D. Catalog of prenatally diagnosed conditions. 3. Aufl. Baltimore: Johns Hopkins University Press, 1999.
Weaver, David D. Catalog of prenatally diagnosed conditions. Baltimore: Johns Hopkins University Press, 1989.
Kuller, Jeffrey A. Prenatal diagnosis & reproductive genetics. St. Louis: Mosby, 1996.
Paley Galst, Joann, und Marion S. Verp, Hrsg. Prenatal and Preimplantation Diagnosis. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-18911-6.
Lilford, Richard. Prenatal diagnosis and prognosis. London: Butterworths, 1990.
Fischmann, Tamara, und Elisabeth Hildt, Hrsg. Ethical Dilemmas in Prenatal Diagnosis. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1396-3.
Buchteile zum Thema "Prental diagnosis":
Atkinson, H. Glenn, und Alan Handyside. „Preimplantation diagnosis“. In Prenatal Diagnosis, 116–33. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-3027-9_8.
Bewley, Susan. „Ethical issues in prenatal diagnosis“. In Prenatal Diagnosis, 1–22. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-3027-9_1.
Bryan, Elizabeth M. „Problems surrounding selective fetocide“. In Prenatal Diagnosis, 149–56. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-3027-9_10.
Statham, Helen. „Parents’ reactions to termination of pregnancy for fetal abnormality: from a mother’s point of view“. In Prenatal Diagnosis, 157–72. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-3027-9_11.
Hall, Ray D. „Parents’ reactions to termination of pregnancy for fetal abnormality: from a father’s point of view“. In Prenatal Diagnosis, 173–80. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-3027-9_12.
White-van Mourik, Margaretha. „Looking in from the outside —“. In Prenatal Diagnosis, 181–201. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-3027-9_13.
Friedrich, Elizabeth. „Caring for the carers“. In Prenatal Diagnosis, 202–12. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-3027-9_14.
Montgomery, Jonathan. „Legal issues in prenatal diagnosis“. In Prenatal Diagnosis, 23–36. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-3027-9_2.
Green, Josephine M. „Women’s experiences of prenatal screening and diagnosis“. In Prenatal Diagnosis, 37–53. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-3027-9_3.
Chapple, Jean. „Screening issues — the public health aspect“. In Prenatal Diagnosis, 54–69. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-3027-9_4.
Konferenzberichte zum Thema "Prental diagnosis":
Forestier, F., F. Daffos, C. Kaplan und P. Champeix. „PRENATAL DIAGNOSIS OF HEMORRHAGIC DISORDERS“. In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644270.
Moodie, P., I. R. Peake, M. B. Liddell und A. L. Bloom. „CARRIER DETECTION AND PRENATAL DIAGNOSIS IN HAEMOPHILIA A BY GENE ANALYSIS“. In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644007.
Lillicrap, D., A. R. Giles, J. J. A. Holden und B. N. White. „THE RELATIVE EFFICACY OF GENETIC ANALYSIS AND COAGULATION TESTING IN THE DIAGNOSIS OF CARRIERS OF HEMOPHILIA A“. In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644010.
Tran, Tram, Susan Mahan, Samantha Spencer, James Kasser und Collin May. „Prenatal Diagnosis of Congenital Lower Extremity Deformity“. In Selection of Abstracts From NCE 2016. American Academy of Pediatrics, 2018. http://dx.doi.org/10.1542/peds.141.1_meetingabstract.640.
Sheehan, Megan M., Ganga Karunamuni, Cameron J. Pedersen, Shi Gu, Yong Qiu Doughman, Michael W. Jenkins, Michiko Watanabe und Andrew M. Rollins. „Prevention of congenital defects induced by prenatal alcohol exposure (Conference Presentation)“. In Diagnosis and Treatment of Diseases in the Breast and Reproductive System III, herausgegeben von Melissa C. Skala und Paul J. Campagnola. SPIE, 2017. http://dx.doi.org/10.1117/12.2253111.
Hadžimuratović, Emina. „PRENATAL IMAGE DIAGNOSIS OF CONGENITAL ANOMALIES OF GASTROINTESTINAL AND URINARY TRACT“. In Međunarodni naučni simpozij FETALNA MEDICINA: OD LEONARDA DA VINCIJA DO DANAS. Akademija nauka i umjetnosti Bosne i Hercegovine, 2015. http://dx.doi.org/10.5644/pi2015-159.07.
Negreskul, Y., K. Burnand, A. Yulia, M. Sellwood, G. Attilakos, P. De Coppi und S. Mitra. „G576(P) Sacrococcygeal teratoma: prenatal diagnosis to post-surgical follow up“. In Royal College of Paediatrics and Child Health, Abstracts of the RCPCH Conference–Online, 25 September 2020–13 November 2020. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2020. http://dx.doi.org/10.1136/archdischild-2020-rcpch.493.
Caris, Elizabeth, Lani Wolfe, Kiana Siefkas, Bailey Brinks und Bhawna Arya. „Resiliency in Families Affected by Prenatal Diagnosis of Congenital Heart Disease“. In AAP National Conference & Exhibition Meeting Abstracts. American Academy of Pediatrics, 2021. http://dx.doi.org/10.1542/peds.147.3_meetingabstract.364.
Faschingbauer, F., S. Wohlfart, T. Goecke, A. Köninger, H. Stepan, R. Gallinat, S. Morris et al. „Accuracy of prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by tooth germ sonography“. In Interdisziplinärer Kongress | Ultraschall 2018 – 42. Dreiländertreffen SGUM | DEGUM | ÖGUM. Georg Thieme Verlag KG, 2018. http://dx.doi.org/10.1055/s-0038-1670428.
de la Salle, C., M. J. Baas, L. Grunebaum, R. Gialeraki, T. Mandalaki und J.-P. Cazenave. „MOLECULAR ANALYSIS OF COAGULATION FACTOR VIII AND IX GENES BY DNA PROBES“. In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643873.