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Screening and familial characterization of copy‐number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure
Authors:Steven M. Harrison  Ian M. Campbell  Melise Keays  Candace F. Granberg  Carlos Villanueva  Grace Tannin  Andrew R. Zinn  Diego H. Castrillon  Chad A. Shaw  Pawel Stankiewicz  Linda A. Baker
Affiliation:1. Department of Urology, University of Texas Southwestern Medical Center, , Dallas, Texas;2. Department of Molecular and Human Genetics, Baylor College of Medicine, , Houston, Texas;3. Department of Pediatrics, University of Texas Southwestern Medical Center, , Dallas, Texas;4. Children's Medical Center at Dallas, , Dallas, Texas;5. Department of Internal Medicine, University of Texas Southwestern Medical Center, , Dallas, Texas;6. McDermott Center for Human Growth and Development, University of Texas Southwestern Medical Center, , Dallas, Texas;7. Department of Pathology, University of Texas Southwestern Medical Center, , Dallas, Texas
Abstract:
Keywords:
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