Nature Genetics
17, 18 - 19 (1997)
doi:10.1038/ng0997-18
Mutations in CDMP1 cause autosomal dominant brachydactyly type CAlexander Polinkovsky1, Nathaniel H. Robin1, 2, 3, J. Terrig Thomas4, Mira Irons5, Audrey Lynn1, Frances R. Goodman6, William Reardon7, Sarina G. Kant8, Han G. Brunner9, Ineke van der Burgt9, David Chitayat10, Julie McGaughran11, Dian Donnai11, Frank P. Luyten4
& Matthew L. Warman1, 2, 3, 12
1Department of Genetics, Case Western Reserve University School of Medicine, 2109 Adelbert Road, Cleveland Ohio 44106, USA.
2Department of Pediatrics, Case Western Reserve University School of Medicine, 2109 Adelbert Road, Cleveland Ohio 44106, USA.
3Center for Human Genetics, University Hospital of Cleveland, Cleveland Ohio, USA.
4Craniofacial and Skeletal Diseases Branch, National Institute of Dental Research, National Institutes of Health, Bethesda Maryland, USA.
5Division of Genetics, Floating Hospital for Children at New England Medical Center, Boston Massachusetts, USA.
6Molecular Medicine Unit, Institute of Child Health, London, UK.
7Mothercare Unit of Clinical Genetics and Fetal Medicine, Institute of Child Health, London, UK.
8Department of Clinical Genetics, University Hospital, Leiden, The Netherlands.
9Department of Clinical Genetics, University Hospital, Nijmegen, The Netherlands.
10Division of Clinical Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
11Department of Clinical Genetics, St. Mary's Hospital, Manchester, UK.
12e-mail: MLW14@po.cwru.edu.
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