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

Mutations inWNT10Aare present in more than half of isolated hypodontia cases

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

Intra-familial Variability of Ectodermal Defects Associated with WNT10A Mutations

(2011) JA McGrath et al.   ACTA DERMATO-VENEREOLOGICA

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

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

Phenotypic variability associated with WNT10A nonsense mutations

(2010) M. Van Geel et al.   BRITISH JOURNAL OF DERMATOLOGY

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

(2010) M Castori et al.   CLINICAL GENETICS

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

(2010) Céline Cluzeau et al.   HUMAN MUTATION

Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A

(2010) Nikoletta Nagy et al.   JOURNAL OF DERMATOLOGICAL SCIENCE

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

EDA Gene Mutations Underlie Non-syndromic Oligodontia

(2009) S. Song et al.   JOURNAL OF DENTAL RESEARCH