B. A. J. Ponder
AuthID: R-00G-3KC
11
TÃTULO: Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delay Full Text
AUTORES: Upadhyaya, M; Ruggieri, M; Maynard, J; Osborn, M; Hartog, C; Mudd, S; Penttinen, M; Cordeiro, I; Ponder, M; Ponder, BAJ; Krawczak, M; Cooper, DN;
PUBLICAÇÃO: 1998, FONTE: HUMAN GENETICS, VOLUME: 102, NÚMERO: 5
AUTORES: Upadhyaya, M; Ruggieri, M; Maynard, J; Osborn, M; Hartog, C; Mudd, S; Penttinen, M; Cordeiro, I; Ponder, M; Ponder, BAJ; Krawczak, M; Cooper, DN;
PUBLICAÇÃO: 1998, FONTE: HUMAN GENETICS, VOLUME: 102, NÚMERO: 5
