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Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
Neuropsychological profile of children and adolescents with the 22q11.2 microdeletionM Woodin, P P Wang, D Aleman, et al.
American Journal of Medical Genetics|August 26, 1998
Further evidence that the Hajdu-Cheney syndrome and the "serpentine fibula-polycystic kidney syndrome" are a single entityF J Ramos, B S Kaplan, R D Bellah, et al.
American Journal of Medical Genetics. Part A|August 30, 2016
Kabuki syndrome as a cause of non-immune fetal hydrops/ascitesAshleigh Long, Elena S Sinkovskaya, Andrew C Edmondson, et al.
Developmental Science|January 14, 2005
Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndromeJoel P Bish, Samantha M Ferrante, Donna McDonald-McGinn, et al.
Clinical Genetics|December 1, 1993
De novo interstitial deletion of the long arm of chromosome 3: 46,XX,del(3)(q25.1q26.1)N H Robin, M Magnusson, D McDonald-McGinn, et al.
American Journal of Human Genetics|December 1, 1999
Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) familiesT H Shaikh, M L Budarf, L Celle, et al.
American Journal of Medical Genetics|February 1, 1984
Recurrence rate for de novo 21q21q translocation Down syndrome: a study of 112 familiesC Steinberg, E H Zackai, D L Eunpu, et al.
Clinical Immunology (Orlando, Fla.)|May 18, 2010
Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)R Zemble, E Luning Prak, K McDonald, et al.
Journal of Medical Genetics|July 1, 1987
De novo 2q+ masquerading as Smith-Lemli-Opitz syndromeA E Donnenfeld, E H Zackai, D M McDonald, et al.
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