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The American Journal of Cardiology|June 1, 1985
Upper limb malformations associated with congenital heart diseaseA E Lin, J K PerloffHuman Molecular Genetics|February 1, 1994
Congenital adrenal hyperplasia caused by a novel homozygous frameshift mutation 273 delta AA in type II 3 beta-hydroxysteroid dehydrogenase gene (HSD3B2) in three male patients of Afghan/Pakistani originJ Simard, E Rhéaume, J F Leblanc, et al.Clinical Genetics|November 18, 2009
Identifying mental health services in clinical genetic settingsM Cappelli, M J Esplen, B J Wilson, et al.Pediatrics|July 4, 1998
Further delineation of aortic dilation, dissection, and rupture in patients with Turner syndromeA E Lin, B Lippe, R G RosenfeldPublic Health Genomics|April 11, 2012
Family history tools in primary care: does one size fit all?B J Wilson, J C Carroll, J Allanson, et al.Public Health Genomics|September 25, 2009
Consent for newborn screening: the attitudes of health care providersF A Miller, R Z Hayeems, J C Carroll, et al.American Journal of Medical Genetics|January 1, 1987
Smith-Lemli-Opitz syndrome-type II: multiple congenital anomalies with male pseudohermaphroditism and frequent early lethalityC J Curry, J C Carey, J S Holland, et al.Clinical Genetics|July 18, 2015
Sixteenth-century German woodcut of a male infant with possible disorganizationT F Heyne, N H Robin, A E LinAmerican Journal of Medical Genetics|November 1, 1990
Central nervous system malformations in the CHARGE associationA E Lin, J R Siebert, J M GrahamPageof 9