MSX1gene polymorphisms in non-syndromic cleft lip and/or palate

Author:

Cardoso ML1,Bezerra JF1,Oliveira GHM1,Soares CD1,Oliveira SR2,de Souza KSC1,da Silva HPV1,Silbiger VN1,Luchessi AD3,Fajardo CM3,Hirata RDC3,Almeida MG1,Hirata MH3,Rezende AA1

Affiliation:

1. Department of Clinical and Toxicological Analysis; School of Pharmaceutical Sciences; Federal University of Rio Grande do Norte; Natal RN Brazil

2. Care Programme for Children with Cleft Lip and Palate; Pediatrics Hospital Professor Heriberto Bezerra; Federal University of Rio Grande do Norte; Natal RN Brazil

3. Department of Clinical and Toxicological Analyses; School of Pharmaceutical Sciences; University of Sao Paulo; São Paulo SP Brazil

Funder

FAPESP

LABMULT/UFRN/RN

LABIOMOL/UFRN/RN

LABMAD/USP/SP

Publisher

Wiley

Subject

General Dentistry,Otorhinolaryngology

Reference50 articles.

1. Msx homeobox gene family and craniofacial development;Alappat;Cell Res,2003

2. Haploview: analysis and visualization of LD and haplotype maps;Barrett;Bioinformatics,2005

3. Testing candidate genes for non-syndromic oral clefts using a case-parent trio design;Beaty;Genet Epidemiol,2002

4. Endogenous Msx1 antisense transcript: in vivo and in vitro evidences, structure, and potential involvement in skeleton development in mammals;Blin-Wakkach;Proc Natl Acad Sci USA,2001

5. Time trends in oral clefts in Chinese newborns: data from the Chinese National Birth Defects Monitoring Network;Dai;Birth Defects Res A Clin Mol Teratol,2010

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