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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. [electronic resource] by
- Upadhyaya, M
- Ruggieri, M
- Maynard, J
- Osborn, M
- Hartog, C
- Mudd, S
- Penttinen, M
- Cordeiro, I
- Ponder, M
- Ponder, B A
- Krawczak, M
- Cooper, D N
Producer: 19980716
In:
Human genetics vol. 102
Availability: No items available.
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