WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population

A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family

(2014) Ebtesam M. Abdalla et al.   ARCHIVES OF ORAL BIOLOGY

WNT10Acoding variants and maxillary lateral incisor agenesis with associated dental anomalies

(2014) Adrianna Mostowska et al.   EUROPEAN JOURNAL OF ORAL SCIENCES

Identification of Genetic Risk Factors for Maxillary Lateral Incisor Agenesis

(2014) M. Alves-Ferreira et al.   JOURNAL OF DENTAL RESEARCH

Taurodontism, variations in tooth number, and misshapened crowns inWnt10anull mice and human kindreds

(2014) Jie Yang et al.   Molecular Genetics & Genomic Medicine

WNT10Amutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations

(2013) Pakeeza Shaiq Arzoo et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

WNT10Amutations also associated with agenesis of the maxillary permanent canines, a separate entity

(2013) P. Kantaputra et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Mutational analysis of AXIN2, MSX1, and PAX9 in two Mexican oligodontia families

(2013) Y.D. Mu et al.   GENETICS AND MOLECULAR RESEARCH

WNT10A variants are associated with non-syndromic tooth agenesis in the general population

(2013) Shujuan Song et al.   HUMAN GENETICS

Candidate Gene Analysis of Tooth Agenesis Identifies Novel Mutations in Six Genes and Suggests Significant Role for WNT and EDA Signaling and Allele Combinations

(2013) Sirpa Arte et al.   PLoS One

Involvement of and Interaction between WNT10A and EDA Mutations in Tooth Agenesis Cases in the Chinese Population

(2013) Huiying He et al.   PLoS One

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

(2012) A Mostowska et al.   CLINICAL GENETICS

Association of common PAX9 variants with permanent tooth size variation in non-syndromic East Asian populations

(2012) Won-Chul Lee et al.   JOURNAL OF HUMAN GENETICS

Mutations inWNT10Aare present in more than half of isolated hypodontia cases

(2012) Marie-José van den Boogaard et al.   JOURNAL OF MEDICAL GENETICS

WNT10A and isolated hypodontia

(2011) Piranit Kantaputra et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes

(2011) Birgitta Bergendal et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Mutational analysis of MSX1 and PAX9 genes in Portuguese families with maxillary lateral incisor agenesis

(2010) Teresa Pinho et al.   EUROPEAN JOURNAL OF ORTHODONTICS

An Arginine Stretch Limits ADAM10 Exit from the Endoplasmic Reticulum

(2010) Elena Marcello et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Investigating the etiology of multiple tooth agenesis in three sisters with severe oligodontia

(2010) S Swinnen et al.   Orthodontics & Craniofacial Research

Mutations in the PAX9 gene in sporadic oligodontia

(2010) E Pawlowska et al.   Orthodontics & Craniofacial Research

WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes

(2009) Axel Bohring et al.   AMERICAN JOURNAL OF HUMAN GENETICS

WNT10A missense mutation associated with a complete Odonto-Onycho-Dermal Dysplasia syndrome

(2009) Sadia Nawaz et al.   EUROPEAN JOURNAL OF HUMAN GENETICS