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SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay
Authors:Yu An  Sami S. Amr  Alcy Torres  Laura Weissman  Peter Raffalli  Gerald Cox  Xiaoming Sheng  Va Lip  Weimin Bi  Ankita Patel  Pawel Stankiewicz  Bai‐Lin Wu  Yiping Shen
Affiliation:1. Institutes of Biomedical Sciences, Children's Hospital and MOE Key Laboratory of Contemporary Anthropology, Fudan University, , Shanghai, China;2. Department of Laboratory Medicine, Boston Children's Hospital, , Boston, Massachusetts;3. Harvard Medical School, , Boston, Massachusetts;4. Brigham and Woman's Hospital, , Boston, Massachusetts;5. Partners Healthcare Center for Personalized Genetic Medicine, , Cambridge, Massachusetts;6. Department of Neurology, Boston Children's Hospital, , Boston, Massachusetts;7. Developmental Medicine Center, Boston Children's Hospital, , Massachusetts;8. Genetics Program, Boston Children's Hospital, Boston, , Massachusetts;9. Department of Molecular and Human Genetics, Baylor College of Medicine, , Houston, Texas;10. Shanghai Children's Medical Center, Jiaotong University School of Medicine, , Shanghai, China
Abstract:
Keywords:20p13  microdeletion  developmental delay  SOX12  NRSN2
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