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Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson–Golabi–Behmel syndrome
Authors:Christina Kehrer  Alexander Hoischen  Ralf Menkhaus  Eva Schwab  Andreas Müller  Sarah Kim  Martina Kreiß  Valerie Weitensteiner  Alina Hilger  Christoph Berg  Anne Geipel  Heiko Reutter  Ulrich Gembruch
Institution:1. Department of Obstetrics and Prenatal Medicine, University of Bonn, Bonn, Germany;2. Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands;3. Center for Assisted Reproduction and Prenatal Diagnosis, Minden, Germany;4. Medical Office for Human Genetics, Wiesbaden, Germany;5. Department of Neonatology and Pediatric Intensive Care, University of Bonn, Bonn, Germany;6. Institute of Human Genetics, University of Bonn, Bonn, Germany;7. Department of Neonatology and Pediatric Intensive Care, University of Bonn, Bonn, Germany

Institute of Human Genetics, University of Bonn, Bonn, Germany

Abstract:
Keywords:
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