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

Mutations inWNT10Aare frequently involved in oligodontia associated with minor signs of ectodermal dysplasia

(2013) Julie Plaisancié et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

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

TBX22 Mutation Associated with Cleft Lip/Palate, Hypodontia, and Limb Anomaly

(2011) Arunee Kaewkhampa et al.   CLEFT PALATE-CRANIOFACIAL JOURNAL

Cleft Lip with Cleft Palate, Ankyloglossia, and Hypodontia are Associated with TBX22 Mutations

(2011) P.N. Kantaputra et al.   JOURNAL OF DENTAL RESEARCH

Polymorphisms in WNT6 and WNT10A and Colorectal Adenoma Risk

(2011) Rachel L. Galbraith et al.   NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL

Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndrome

(2010) Warissara Sripathomsawat et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

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

Management of Dens Invaginatus Type I and Open Apex: Report of Three Cases

(2010) Márcia S. Schmitz et al.   JOURNAL OF ENDODONTICS

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

Genetic basis of tooth agenesis

(2009) Pekka Nieminen   JOURNAL OF EXPERIMENTAL ZOOLOGY PART B-MOLECULAR AND DEVELOPMENTAL EVOLUTION