✦ LIBER ✦
Mutation screening of EXT1 and EXT2 by direct sequence analysis and MLPA in patients with multiple osteochondromas: splice site mutations and exonic deletions account for more than half of the mutations
✍ Scribed by Vink, Geraldine R; White, Stefan J; Gabelic, Strelicija; Hogendoorn, Pancras C W; Breuning, Martijn H; Bakker, Egbert
- Book ID
- 110026148
- Publisher
- Nature Publishing Group
- Year
- 2004
- Tongue
- English
- Weight
- 74 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1018-4813
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