![](/img/cover-not-exists.png)
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
Sylvia Bruneau, Kenneth R. Johnson, Masakazu Yamamoto, Atsushi Kuroiwa, Denis DubouleVolume:
237
Year:
2001
Language:
english
Pages:
354
DOI:
10.1006/dbio.2001.0382
File:
PDF, 364 KB
english, 2001