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HLX is a candidate gene for a pattern of anomalies associated with congenital diaphragmatic hernia,short bowel,and asplenia
Authors:Sandra A. Farrell  Sandi Sodhi  Christian R. Marshall  Andrea Guerin  Anne Slavotinek  Tara Paton  Karen Chong  Wilma L. Sirkin  Stephen W. Scherer  Félix‐Antoine Bérubé‐Simard  Nicolas Pilon
Affiliation:1. Department of Laboratory Medicine and Genetics, Trillium Health Partners, Mississauga, Ontario, Canada;2. Genome Diagnostics, Department of Pediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada;3. The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada;4. Division of Clinical Genetics and Metabolics, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada;5. Division of Medical Genetics, Department of Pediatrics, Kingston General Hospital, Kingston, Ontario, Canada;6. Department of Pediatrics, University of California San Francisco, San Francisco, California;7. Prenatal Diagnosis and Medical Genetics Program, Department of Obstetrics and Gynecology, Mount Sinai Hospital, Toronto, Ontario, Canada;8. Department of Laboratory Medicine, North York General Hospital, Department of Laboratory Medicine and Pathology, University of Toronto, Toronto, Ontario, Canada;9. Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada;10. Department of Molecular Genetics and McLaughlin Centre, University of Toronto, Toronto, Ontario, Canada;11. Molecular Genetics of Development Laboratory, Department of Biological Sciences and BioMed Research Center, Faculty of Sciences, University of Quebec at Montreal, Montreal, Quebec
Abstract:
Keywords:asplenia  autosomal recessive  congenital diaphragmatic hernia  congenital short bowel
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