Screening of mutations in thePHF8gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palate

Author:

Koivisto AM,Ala-Mello S,Lemmelä S,Komu HA,Rautio J,Järvelä I

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference13 articles.

1. X-linked mental retardation: further lumping, splitting and emerging phenotypes;Kleefstra;Clin Genet,2005

2. X-linked mental retardation;Ropers;Nat Rev Genet,2005

3. Monogenic X-linked mental retardation: is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutations;Mandel;Eur J Hum Genet,2004

4. Three new families with X-linked mental retardation caused by the 428-451dup(24bp) mutation in ARX;Partington;Clin Genet,2004

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