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Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths
Authors:R. Alan Harris  Francesca Ferrari  Shay Ben-Shachar  Xiaoling Wang  George Saade  Ignatia Van Den Veyver  Fabio Facchinetti  Kjersti Aagaard-Tillery
Affiliation:1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA

Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, TX, USA;2. Department of Obstetrics and Gynecology, UTMB-Galveston, Galveston, TX, USA

Unit of Obstetrics and Gynecology, University of Modena and Reggio Emilia, Modena, Italy;3. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA;4. Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, TX, USA;5. Department of Obstetrics and Gynecology, UTMB-Galveston, Galveston, TX, USA;6. Unit of Obstetrics and Gynecology, University of Modena and Reggio Emilia, Modena, Italy

Abstract:
Keywords:stillbirth  copy number variants  deletion syndromes  duplication syndromes  fetal death
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