论文信息 - Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain - 字舞流文

Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain

T. Roscioli | T. Cox | A. Bankier | G. McGillivray | R. Savarirayan | R. Gardner | J. Bateman | S. Lamandé | R. McNeil | C. Stojkoski