Richard M. Goodman Fellowship: A research fellowship in Jewish Genetic Diseases
- 作者Robert J. Gorlin
- 卷第40卷
- 期第1期
- 印刷ISSN1552-4825
- 电子ISSN1552-4833
- 文件大小67.95KB
- 发表时间1991
- DOI10.1002/ajmg.1320400132
- 页码131-131
New somatic cell hybrids for physical mapping in distal Xq and the fragile X regionSusan A. Ledbetter; Charles E. Schwartz; Kay E. Davies; Dr. David H. Ledbetter · 1991
Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomalyDr. Frank Greenberg; Kristine B. Courtney; Robert A. Wessels; Dr. James Huhta; Robert J. Carpenter; Donna C. Rich; David H. Ledbetter; John M. Opitz; James F. Reynolds · 1988
Second Annual Prader-Willi Syndrome Scientific ConferenceDr. David H. Ledbetter; Frank Greenberg; Vanja A. Holm; Suzanne B. Cassidy; John M. Opitz; James F. Reynolds · 1987
Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17Frank Greenberg; Robert F. Stratton; Lillian H. Lockhart; Frederick F. B. Elder; William B. Dobyns; Dr. David H. Ledbetter; John M. Opitz; James F. Reynolds · 1986
Risk factors associated with transcervical CVS lossesDr Mitchell S. Golbus; Joe Leigh Simpson; Sarah E. Fowler; Felix de la Cruz; Robert J. Desnick; Ronald Wapner; David H. Ledbetter; Herbert Lubs; Maurice J. Mahoney; Eugene Pergament; George G. Rhoads; Joseph D. Schulman; Julia Zachary · 1992
Cloning and characterization of the T(15;17) translocation breakpoint region in acute promyelocytic leukemiaDr. Richard S. Lemons; David Eilender; Richard A. Waldmann; Matt Rebentisch; Ann-Kristin Frej; David H. Ledbetter; Cheryl Willman; Thomas McConnell; Peter O'Connell · 1990
Duplication of proximal 15q as a cause of Prader-Willi syndromeAnjana L. Pettigrew; Susanne M. Gollin; Frank Greenberg; Vincent M. Riccardi; Dr. David H. Ledbetter; John M. Opitz; James F. Reynolds · 1987