Condition: TOOTH AGENESIS, SELECTIVE, 4 (disorder)


rs146460077 in LOC107984111;WNT10A gene and TOOTH AGENESIS, SELECTIVE, 4 (disorder) PMID 27657131 2016 Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients.

PMID 22581971 2012 Mutations in WNT10A are present in more than half of isolated hypodontia cases.

PMID 29178643 2017 Role of WNT10A in failure of tooth development in humans and zebrafish.

PMID 24311251 2014 WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity.

PMID 23401279 2013 Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.

PMID 21484994 2011 WNT10A and isolated hypodontia.

PMID 20979233 2011 Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.

PMID 24449199 2014 WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations.

rs121908120 in WNT10A gene and TOOTH AGENESIS, SELECTIVE, 4 (disorder) PMID 29178643 2017 Role of WNT10A in failure of tooth development in humans and zebrafish.

PMID 20979233 2011 Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.

PMID 24311251 2014 WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity.

PMID 27657131 2016 Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients.

PMID 22581971 2012 Mutations in WNT10A are present in more than half of isolated hypodontia cases.

PMID 23401279 2013 Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.

PMID 24449199 2014 WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations.

PMID 21484994 2011 WNT10A and isolated hypodontia.

PMID 19559398 2009 WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

PMID 21143469 2011 Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum.

PMID 19471313 2009 WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome.

PMID 22670871 2013 Late diagnosis of ectodermal dysplasia syndrome.

PMID 24902757 2014 Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.

PMID 20163410 2010 Phenotypic variability associated with WNT10A nonsense mutations.

PMID 23167694 2013 Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.

PMID 28981473 2017 Novel EDA or EDAR Mutations Identified in Patients with X-Linked Hypohidrotic Ectodermal Dysplasia or Non-Syndromic Tooth Agenesis.

rs121908119 in WNT10A;LOC107984111 gene and TOOTH AGENESIS, SELECTIVE, 4 (disorder) PMID 25545742 2015 WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies.

PMID 24902757 2014 Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.

PMID 19559398 2009 WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

PMID 24702986 2014 Dento-maxillo-facial phenotype and implants-based oral rehabilitation in Ectodermal Dysplasia with WNT10A gene mutation: report of a case and literature review.

PMID 24398796 2014 Variability in dentofacial phenotypes in four families with WNT10A mutations.

PMID 23167694 2013 Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.

PMID 25629078 2015 Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.