A comparative phenotypic study of kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 or prokineticin receptor 2 genes.
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P. Tonella | B. Conrad | J. Hardelin | Jacques Young | I. Arnulf | G. Reach | S. Jacquemont | C. Bouvattier | P. Rondard | C. Dodé | B. Delobel | N. Chabbert-Buffet | M. Mathieu | S. Cabrol | S. Wołczyński | J. Lespinasse | S. Brailly‐Tabard | M. Pugeat | T. Brue | M. Bidet | P. Bouchard | A. Lienhardt-Roussie | M. Ramos-Arroyo | A. Guiochon‐Mantel | A. Murat | J. Sarfati | C. Brémont | G. Morgan | F. Despert | Z. Turki | H. Du Boullay | Alfonso García-Piñero | Nicole de Talence