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Camptodactyly and the 22q11.2 deletion syndrome
Authors:Natario L. Couser  Chetna K. Pande  Jonathan M. Walsh  James Tepperberg  Arthur S. Aylsworth
Affiliation:1. Department of Pediatrics, Division of Genetics and Metabolism, School of Medicine, University, of North Carolina at Chapel Hill, Chapel Hill, North Carolina;2. Department of Ophthalmology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina;3. Texas Tech Health Sciences Center, Paul L. Foster School of Medicine, El Paso, Texas;4. Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland;5. Department of Otolaryngology/Head and Neck Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina;6. Department of Otolaryngology/Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland;7. LabCorp, Research Triangle Park, North Carolina;8. Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina
Abstract:
Keywords:camptodactyly  laryngeal web  sub‐glottic stenosis  laryngomalacia  22q11 microdeletion syndrome (22q11.2DS)  DiGeorge syndrome (DGS)  velocardiofacial syndrome (VCFS)
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