Deborah A. Driscoll

Evidence for a genetic basis for hyperandrogenemia in polycystic ovary syndrome

Richard S. Legro, Deborah A. Driscoll, Jerome F. Strauss et al. · Proceedings of the National Academy of Sciences · 1998 · 697 citations · Full text

Frequency of 22q11 deletions in patients with conotruncal defects

Elizabeth Goldmuntz, Bernard J. Clark, Laura E. Mitchell et al. · Journal of the American College of Cardiology · 1998 · 587 citations · Full text

Thirty-seven candidate genes for polycystic ovary syndrome: Strongest evidence for linkage is with follistatin

Margrit Urbanek, Richard S. Legro, Deborah A. Driscoll et al. · Proceedings of the National Academy of Sciences · 1999 · 491 citations

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.

Deborah A. Driscoll, J Salvin, Beatrice Sellinger et al. · Journal of Medical Genetics · 1993 · 488 citations · Full text

Genetics, Genetic Epidemiology, Gynecology +19

Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel

Michael S. Watson, Garry R. Cutting, Robert J. Desnick et al. · Genetics in Medicine · 2004 · 450 citations · Full text

Genetic Testing, Genetic Disorder, Medicine +8