The Molecular Basis of X-Linked Spondyloepiphyseal Dysplasia Tarda

The American Journal of Human Genetics - Tập 68 - Trang 1386-1397 - 2001
A.K. Gedeon1,2, G.E. Tiller3, M. Le Merrer4, S. Heuertz4, L. Tranebjaerg5, D. Chitayat6, S. Robertson7, I.A. Glass8,9, R. Savarirayan7,10, W.G. Cole6, D.L. Rimoin11, B.G. Kousseff12, H. Ohashi13, B. Zabel14, A. Munnich15, J. Gecz1,2, J.C. Mulley1,16
1Centre for Medical Genetics, Department of Cytogenetics and Molecular Genetics, Women’s and Children’s Hospital, University of Adelaide, Adelaide
2Department of Paediatrics, Adelaide
3Vanderbilt University School of Medicine, Nashville
4Institute Necker Malades, Paris
5Department of Medical Genetics, University Hospital of Tromso, Tromso, Norway
6Hospital for Sick Children, Toronto
7Victorian Clinical Genetics Service University of Melbourne, Melbourne
8Queensland Clinical Genetics Service and University of Queensland School of Medicine, Brisbane
9Medical Genetics, University of Washington-CHRMC, Seattle
10University of Melbourne Department of Paediatrics, Melbourne
11Cedars-Sinai Medical Center, Los Angeles
12University of South Florida, Tampa
13Saitama Children’s Medical Centre, Saitama, Japan
14University of Mainz, Mainz, Germany
15INSERM U393, Hopital Necker-Enfants Malades, Paris
16Department of Genetics, Adelaide

Tài liệu tham khảo

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