Showing results (21-30 of 83) with videos related to
Sort By:
Pageof 9
Journal of Intellectual Disability Research : JIDR|February 13, 2019
Fragile X syndrome clinical trials: exploring parental decision-makingC S D'Amanda, H L Peay, A C Wheeler, et al.Genome Research|September 14, 2000
Rapid detection of deletion, insertion, and substitution mutations via heteroduplex analysis using capillary- and microchip-based electrophoresisH Tian, L C Brody, J P LandersAmerican Journal of Human Genetics|June 1, 1990
Report of the 1989 Asilomar meeting on education in genetic counselingA P Walker, J A Scott, B B Biesecker, et al.Breast Disease|February 3, 2005
New approaches to BRCA1 mutation detectionJ G Hacia, L C Brody, F S CollinsMolecular Psychiatry|December 19, 1998
Applications of DNA chips for genomic analysisJ G Hacia, L C Brody, F S CollinsAnalytical Chemistry|November 18, 2000
Effective capillary electrophoresis-based heteroduplex analysis through optimization of surface coating and polymer networksH Tian, L C Brody, D Mao, et al.Human Mutation|August 3, 2000
The breast cancer information core: database design, structure, and scopeC Szabo, A Masiello, J F Ryan, et al.Human Molecular Genetics|November 1, 1993
Expression and processing of human ornithine-delta-aminotransferase in Saccharomyces cerevisiaeK M Dougherty, D A Swanson, L C Brody, et al.Human Molecular Genetics|September 1, 1996
KVLQT1 mutations in three families with familial or sporadic long QT syndromeM W Russell, M Dick, F S Collins, et al.Clinical Genetics|September 17, 2013
Parental attitudes, values, and beliefs toward the return of results from exome sequencing in childrenJ C Sapp, D Dong, C Stark, et al.Pageof 9