Screening of mutations in thePHF8gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palate
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2007.00836.x/fullpdf
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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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