论文信息 - Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. - 字舞流文

Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

M. Tekin | J. Gusella | S. Eom | Hyung-Goo Kim | W. Wenzel | Yang Shi | D. Bick | I. Meliciani | F. Lan | G. Rosenberger | L. Layman | I. Kurth | G. B. Kang | Steven L. Walker | M. Ozata | R. Sherins