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Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registry
Authors:Siddharth K. Prakash  Carolyn A. Bondy  Cheryl L. Maslen  Michael Silberbach  Angela E. Lin  Laura Perrone  Giuseppe Limongelli  Hector I. Michelena  Eduardo Bossone  Rodolfo Citro  BAVCon Investigators  GenTAC Registry Investigators  Scott A. Lemaire  Simon C. Body  Dianna M. Milewicz
Affiliation:1. Division of Medical Genetics, Department of Internal Medicine, University of Texas Health Science Center at Houston, Houston, Texas;2. Correspondence to:;3. Siddharth Prakash, M.D., Ph.D., Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, 6431 Fannin Street, MSB 6.106, Houston, TX 77030.;4. E‐mail:;5. National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland;6. Departments of Molecular and Medical Genetics and Pediatrics, Oregon Health & Science University, Portland, Oregon;7. Department of Medical Genetics, MassGeneral Hospital for Children, Boston, Massachusetts;8. Department of Pediatrics “F. Fede”, Seconda Università degli Studi di Napoli, Naples, Italy;9. Division of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota;10. Department of Cardiology and Cardiac Surgery, University Hospital “Scuola Medica Salernitana”, Salerno, Italy;11. Division of Cardiothoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas;12. Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts
Abstract:
Keywords:genomics  Turner syndrome  valvular heart disease  congenital heart defects  X chromosome
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