Reassessing the clinical spectrum associated with hereditary leiomyomatosis and renal cell carcinoma syndrome in French FH mutation carriers
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C. Genestie | S. Richard | Y. Allory | G. Le Teuff | B. Escudier | A. Gimenez-Roqueplo | B. Bressac-de Paillerets | N. Soufir | M. Avril | A. Slama | N. Poulalhon | M. Guillaud-Bataille | S. Deveaux | L. Albiges | P. Benusiglio | B. Gardie | C. Saldana | S. Ferlicot | M. Muller