SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome
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J. Hardelin | Jacques Young | C. Cruaud | C. Dodé | V. Prévot | S. Baron | K. Geršak | D. Dewailly | P. Giacobini | J. Parkash | V. Meyer | Charlotte Vanacker | N. Hanchate | C. Espy | M. Pugeat | F. Collier | G. Chabrier | C. Metz | C. Cortet-Rudelli | C. Leroy | C. Campagne | P. Lhuillier | Corinne Fouveaut | Alfonso García-Piñero | N. K. Hanchate