✦ LIBER ✦
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
✍ Scribed by M. Upadhyaya; M. Ruggieri; J. Maynard; M. Osborn; C. Hartog; S. Mudd; M. Penttinen; I. Cordeiro; M. Ponder; B. A. J. Ponder; M. Krawczak; D. N. Cooper
- Book ID
- 106136960
- Publisher
- Springer
- Year
- 1998
- Tongue
- English
- Weight
- 119 KB
- Volume
- 102
- Category
- Article
- ISSN
- 0340-6717
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