Polymorphisms in FGF12, VCL, CX43 and VAX1in Brazilian patients with nonsyndromic cleft lip with or without cleft palate

Polymorphisms at Regions 1p22.1 (rs560426) and 8q24 (rs1530300) Are Risk Markers for Nonsyndromic Cleft Lip and/or Palate in the Brazilian Population

(2013) Elizabete Bagordakis et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population

(2012) Luciano A. Brito et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Connexins in atherosclerosis

(2012) Anna Pfenniger et al.   BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES

Resequencing ofVAX1in patients with nonsyndromic cleft lip with or without cleft palate

(2012) Entessar Nasser et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil

(2012) Luciano Abreu Brito et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Cleft Lip in Oculodentodigital Dysplasia Suggests Novel Roles for Connexin43

(2012) K. Amano et al.   JOURNAL OF DENTAL RESEARCH

Roles of intracellular fibroblast growth factors in neural development and functions

(2012) Xu Zhang et al.   Science China-Life Sciences

Genetics of Nonsyndromic Orofacial Clefts

(2011) Fedik Rahimov et al.   CLEFT PALATE-CRANIOFACIAL JOURNAL

VAX1mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: The first description of aVAX1phenotype in humans

(2011) Anne M. Slavotinek et al.   HUMAN MUTATION

Cleft lip and palate: understanding genetic and environmental influences

(2011) Michael J. Dixon et al.   NATURE REVIEWS GENETICS

The Genomic Ancestry of Individuals from Different Geographical Regions of Brazil Is More Uniform Than Expected

(2011) Sérgio D. J. Pena et al.   PLoS One

Fetal genetic risk of isolated cleft lip only versus isolated cleft lip and palate: A subphenotype analysis using two population-based studies of orofacial clefts in scandinavia

(2010) Astanand Jugessur et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Ethnic Heterogeneity of IRF6 AP-2a Binding Site Promoter SNP Association with Nonsyndromic Cleft Lip and Palate

(2010) Susan H. Blanton et al.   CLEFT PALATE-CRANIOFACIAL JOURNAL

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

(2010) Terri H Beaty et al.   NATURE GENETICS

Replication of two novel susceptibility loci for non-syndromic orofacial clefts in a Chinese population

(2010) Y Pan et al.   ORAL DISEASES

IRF6gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate

(2009) Stefanie Birnbaum et al.   EUROPEAN JOURNAL OF ORAL SCIENCES

GJA1mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

(2009) William A. Paznekas et al.   HUMAN MUTATION

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

(2009) Elisabeth Mangold et al.   NATURE GENETICS

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24

(2009) Stefanie Birnbaum et al.   NATURE GENETICS

Lack of association betweenIRF6polymorphisms (rs2235371 and rs642961) and non-syndromic cleft lip and/or palate in a Brazilian population

(2009) LMR Paranaíba et al.   ORAL DISEASES

Prevalence of orofacial clefts and social factors in Brazil

(2009) Katamara Rodrigues et al.   Brazilian Oral Research

Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip

(2008) Fedik Rahimov et al.   NATURE GENETICS