Multiple congenital malformations of Wolf-Hirschhorn syndrome are recapitulated in<i>Fgfrl1</i>null mice
Wolf-Hirschhorn syndrome (WHS) is caused by deletions in the short arm of chromosome 4 (4p) and occurs in about one per 20,000 births. Patients with WHS display a set of highly variable characteristics including craniofacial dysgenesis, mental retardation, speech problems, congenital heart defects,...
Saved in:
| Main Authors: | , , , , , |
|---|---|
| 格式: | Artigo |
| 語言: | 英语 |
| 出版: |
2009
|
| 在線閱讀: | https://doi.org/10.1242/dmm.002287 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|