✦ LIBER ✦
The Mouse Hoxd13spdh Mutation, a Polyalanine Expansion Similar to Human Type II Synpolydactyly (SPD), Disrupts the Function but Not the Expression of Other Hoxd Genes
✍ Scribed by Sylvia Bruneau; Kenneth R. Johnson; Masakazu Yamamoto; Atsushi Kuroiwa; Denis Duboule
- Book ID
- 115598813
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 364 KB
- Volume
- 237
- Category
- Article
- ISSN
- 0012-1606
No coin nor oath required. For personal study only.