WNT10A and isolated hypodontia

Phenotypic variability associated with WNT10A nonsense mutations

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

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

Reciprocal Requirements for EDA/EDAR/NF-κB and Wnt/β-Catenin Signaling Pathways in Hair Follicle Induction

(2009) Yuhang Zhang et al.   DEVELOPMENTAL CELL

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

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

Wnt/β-catenin signaling directs multiple stages of tooth morphogenesis

(2007) Fei Liu et al.   DEVELOPMENTAL BIOLOGY