Gene/environment causes of cleft lip and/or palate
Top Cited Papers
- 1 April 2002
- journal article
- review article
- Published by Wiley in Clinical Genetics
- Vol. 61 (4) , 248-256
- https://doi.org/10.1034/j.1399-0004.2002.610402.x
Abstract
Craniofacial anomalies, and in particular cleft lip and palate, are major human birth defects with a worldwide frequency of 1 in 700 and substantial clinical impact. A wide range of studies in develo...Keywords
This publication has 106 references indexed in Scilit:
- Linkage disequilibrium between GABRB3 gene and nonsyndromic familial cleft lip with or without cleft palateHuman Genetics, 2001
- Analysis of the candidate genes responsible for non-syndromic cleft lip and palate in Japanese peopleClinical Science, 2000
- Maternal risk factors in cleft lip and palate: case control studyBritish Journal of Oral and Maxillofacial Surgery, 2000
- Role of the C677T polymorphism at theMTHFR gene on risk to nonsyndromic cleft lip with/without cleft palate: Results from a case-control study in BrazilAmerican Journal of Medical Genetics, 1999
- Differential expression and biological activity of retinoic acid-induced TGFβ isoforms in embryonic palate mesenchymal cellsJournal of Cellular Physiology, 1998
- A Locus in 2p13–p14 (OFC2), in Addition to That Mapped in 6p23, Is Involved in Nonsyndromic Familial Orofacial Cleft MalformationGenomics, 1998
- No evidence of linkage between the transforming growth factor-alpha gene in families with apparently autosomal dominant inheritance of cleft lip and palate.Journal of Medical Genetics, 1992
- Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6Clinical Genetics, 1987
- Retinoic Acid EmbryopathyNew England Journal of Medicine, 1985