R. Veitia
AuthID: R-00F-FEC
1
TITLE: 46,XY complete gonadal dysgenesis (Sywers Syndrome) and 46,XY partial gonadal dysgenesis associated with deletions of 9p Full Text
AUTHORS: Veitia, R; Goncalves, J; Silva, M; Rodrigues, JC; Boieiro, F; Marques, R; Lavinha, J; Caspurro, M; Nunes, M; Rappaport, R; Thibaud, E; Jaubert, F; Fellous, M; McElreavey, K;
PUBLISHED: 1998, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 6
AUTHORS: Veitia, R; Goncalves, J; Silva, M; Rodrigues, JC; Boieiro, F; Marques, R; Lavinha, J; Caspurro, M; Nunes, M; Rappaport, R; Thibaud, E; Jaubert, F; Fellous, M; McElreavey, K;
PUBLISHED: 1998, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 6
INDEXED IN: 
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