Association of MEOX2 polymorphism with nonsyndromic cleft palate only in a Vietnamese population

Author:

Tran Duy L.12ORCID,Imura Hideto134,Mori Akihiro134,Suzuki Satoshi134,Niimi Teruyuki134,Ono Maya134,Sakuma Chisato134,Nakahara Shinichi1,Nguyen Tham T.H.12,Pham Phuong T.2,Hoang Viet2,Tran Van T.T.5,Nguyen Minh D.5,Natsume Nagato134

Affiliation:

1. Division of Research and Treatment for Oral Maxillofacial Congenital Anomalies; Aichi Gakuin University; Nagoya Japan

2. Nguyen Dinh Chieu General Hopsital; Ben Tre Vietnam

3. Cleft Lip and Palate Center, Aichi Gakuin Dental Hospital; Nagoya Japan

4. Division of Speech, Hearing, and Language; Aichi Gakuin Dental Hospital; Nagoya Japan

5. Odonto and Maxillofacial Hospital; Ho Chi Minh Vietnam

Funder

Japan Society for the Promotion of Science

Grant-in-Aid for Challenging Exploratory Research

Grant-in-Aid for Scientific Research

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Reference55 articles.

1. OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders

2. Haploview: Visualization and analysis of SNP genotype data;Barrett;Cold Spring Harbor Protocols,2009

3. Epidemiology, etiology, and treatment of isolated cleft palate;Burg;Front Physiol,2016

4. Folic acid supplementation use and the MTHFR C677T polymorphism in orofacial clefts etiology: An individual participant data pooled-analysis;Butali;Birth Defects Res A Clin Mol Teratol,2013

5. Mox-1 and Mox-2 define a novel homeobox gene subfamily and are differentially expressed during early mesodermal patterning in mouse embryos;Candia;Development,1992

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