Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations
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M. Hauschild | P. Bouloux | M. Polak | T. Raivio | M. Mohammadi | V. Drouin‐Garraud | M. Gérard | N. de Roux | J. Carel | Yang Liu | G. Sykiotis | D. Tiosano | N. Pitteloud | A. Dwyer | Cheng Xu | J. Léger | Y. Sidis | L. Plummer | J. Tommiska | H. Lefebvre | C. Villanueva | S. Manouvrier | F. Phan-Hug | A. Beenken | Youli Hu | Elka E Jacobson-Dickman | J. Rey | F. Phan‐Hug | Elka E. Jacobson-Dickman