Screening of mutations in the PHF8 gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palate
✍ Scribed by AM Koivisto; S Ala-Mello; S Lemmelä; HA Komu; J Rautio; I Järvelä
- Book ID
- 110888430
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 322 KB
- Volume
- 72
- Category
- Article
- ISSN
- 0009-9163
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## Abstract ## BACKGROUND Human nonsyndromic cleft lip and palate, CL(P), is genetically complex, with one contributing gene on chromosome 17q. A potentially homologous gene, __clf1__ on distal chromosome 11, is part of the digenic cause of the 10–30% CL(P) in the A/WySn mouse strain. Here we repo