Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis.
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E. Zackai | S. Twigg | A. Wilkie | A. Verloes | M. Muenke | S. Tomkins | D. McDonald-McGinn | J. Cook | David W. Johnson | S. Wall | S. Kan | E. Reich | N. Elanko | L. Cornejo-Roldán | S. Rannan-Eliya | David Johnson | J. Cook | Shih-hsin Kan