Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development
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J. Weissenbach | A. Munnich | C. Cruaud | M. Gonzalès | S. Lyonnet | M. Vekemans | F. Encha-Razavi | J. Amiel | J. Martinovic | T. Attié-Bitach | H. Etchevers | M. Clément-Ziza | C. Ozilou | D. Sanlaville | A. Pelet | C. Esculpavit | S. Audollent | G. Goudefroye | A. Delezoide | M. Aubry | N. Morichon‐Delvallez | Y. Dumez | C. Fredouille | N. Joyē | S. Chemouny | Arnold Munnich | Géraldine Goudefroye