Showing results (1-10 of 20) with videos related to
Sort By:
Pageof 2
Canadian Family Physician Medecin De Famille Canadien|January 22, 2011
Genetic disorders in the newborn infantW S Meschino, A M SummersAmerican Journal of Medical Genetics|December 18, 2001
Ethical, legal, and practical concerns about recontacting patients to inform them of new information: the case in medical geneticsA G Hunter, N Sharpe, M Mullen, et al.Clinical Genetics|May 26, 2017
Disruption of YWHAE gene at 17p13.3 causes learning disabilities and brain abnormalitiesA Noor, S Bogatan, N Watkins, et al.Nature Genetics|December 30, 1999
Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletionL Potocki, K S Chen, S S Park, et al.American Journal of Medical Genetics|July 23, 1998
Schimke immunoosseous dysplasia complicated by moyamoya phenomenonC F Boerkoel, M J Nowaczyk, S I Blaser, et al.Clinical Genetics|June 14, 2000
Perceptions of Ashkenazi Jewish breast cancer patients on genetic testing for mutations in BRCA1 and BRCA2K A Phillips, E Warner, W S Meschino, et al.Journal of Medical Genetics|March 1, 1993
Interstitial deletion of chromosome 10q23: a new case and reviewS A Farrell, W Szymonowicz, G Chow, et al.Prenatal Diagnosis|December 15, 2005
The influence of risk estimates obtained from maternal serum screening on amniocentesis ratesV M Mueller, T Huang, A M Summers, et al.Prenatal Diagnosis|December 15, 2005
The effect of fetal gender on the false-positive rate of Down syndrome by maternal serum screeningV M Mueller, T Huang, A M Summers, et al.Journal of Medical Screening|October 17, 2003
Maternal serum screening in Ontario using the triple marker testA M Summers, S A Farrell, T Huang, et al.Pageof 2