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,...
保存先:
| 主要な著者: | , , , , , |
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| フォーマット: | Artigo |
| 言語: | 英語 |
| 出版事項: |
2009
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| オンライン･アクセス: | https://doi.org/10.1242/dmm.002287 |
| タグ: |
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