B. A. J. Ponder
AuthID: R-00G-3KC
11
TITLE: 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
AUTHORS: Upadhyaya, M; Ruggieri, M; Maynard, J; Osborn, M; Hartog, C; Mudd, S; Penttinen, M; Cordeiro, I; Ponder, M; Ponder, BAJ; Krawczak, M; Cooper, DN;
PUBLISHED: 1998, SOURCE: HUMAN GENETICS, VOLUME: 102, ISSUE: 5
AUTHORS: Upadhyaya, M; Ruggieri, M; Maynard, J; Osborn, M; Hartog, C; Mudd, S; Penttinen, M; Cordeiro, I; Ponder, M; Ponder, BAJ; Krawczak, M; Cooper, DN;
PUBLISHED: 1998, SOURCE: HUMAN GENETICS, VOLUME: 102, ISSUE: 5
