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American Journal of Medical Genetics|August 1, 1987
Lymphedema in Noonan syndrome: clues to pathogenesis and prenatal diagnosis and review of the literatureD R Witt, H E Hoyme, J Zonana, et al.
Lancet (London, England)|March 11, 1978
Prenatal diagnosis of homozygous familial hypercholesterolaemia. Expression of a genetic receptor disease in uteroM S Brown, P T Kovanen, J L Goldstein, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Predictive testing for Huntington's disease: risk perception, reasons for testing and psychological profile of test applicantsM Decruyenaere, G Evers-Kiebooms, A Boogaerts, et al.
Cancer Genetics and Cytogenetics|July 1, 1993
Endometrial polyp: another benign tumor characterized by 12q13-q15 changesR Vanni, P Dal Cin, S Marras, et al.
Virchows Archiv : an International Journal of Pathology|August 30, 2000
Multifocal epithelioid angiosarcoma of the small intestineV Delvaux, R Sciot, B Neuville, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|May 10, 2006
Neoadjuvant chemotherapy followed by radical hysterectomy for invasive cervical cancer diagnosed during pregnancy: report of a case and review of the literatureS Caluwaerts, K VAN Calsteren, L Mertens, et al.
Journal of Medical Genetics|June 9, 2009
17q21.31 microduplication patients are characterised by behavioural problems and poor social interactionB Grisart, L Willatt, A Destrée, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpointP Debeer, E F Schoenmakers, R Thoelen, et al.
American Journal of Medical Genetics|February 25, 1998
Pfeiffer syndrome type 2: further delineation and review of the literatureA S Plomp, B C Hamel, J M Cobben, et al.
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