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Nature Genetics  29, 107 - 109 (2001)
doi:10.1038/ng1001-107

Time for T

Jeffrey C. Murray

Department of Pediatrics, University of Iowa, Iowa City, Iowa 52242, USA. jeff-murray@uiowa.edu

Genetic defects responsible for cleft lip and cleft palate are only now beginning to be uncovered. Mutations in the gene encoding a T-box transcription factor have been identified as the cause of the rare X-linked syndrome cleft palate with tongue-tie. And in another study, heterozygotes for a defective allele for a cell adhesion molecule, which is responsible for a rare clefting syndrome when homozygous, have been found at higher than expected incidence in sporadic forms of clefting.

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RESEARCH
Mutation of PVRL1 is associated with sporadic, non-syndromic cleft lip/palate in northern Venezuela
Nature Genetics Brief Communication (01 Oct 2001)
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia
Nature Genetics Letters (01 Oct 2001)
Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia
Nature Genetics Letters (01 Aug 2000)
Tbx3 impinges on the p53 pathway to suppress apoptosis, facilitate cell transformation and block myogenic differentiation
Oncogene Original Article (29 May 2002)

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Nature Genetics
ISSN: 1061-4036
EISSN: 1546-1718
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