A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia

Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia

(2014) Singwai Wong et al.   ARCHIVES OF ORAL BIOLOGY

A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia

(2014) S.-W. Wong et al.   MUTAGENESIS

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

Developmental disorders of the dentition: An update

(2013) Ophir D. Klein et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

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

Non-syndromic Tooth Agenesis Associated with a Nonsense Mutation in Ectodysplasin-A (EDA)

(2013) T. Nikopensius et al.   JOURNAL OF DENTAL RESEARCH

Novel EDA p.Ile260Ser Mutation Linked to Non-syndromic Hypodontia

(2013) Y. Yang et al.   JOURNAL OF DENTAL RESEARCH

Genetic background of nonsyndromic oligodontia: a systematic review and meta-analysis

(2013) S. Ruf et al.   Journal of Orofacial Orthopedics-Fortschritte der Kieferorthopadie

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

Molecular patterning of the mammalian dentition

(2013) Yu Lan et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

The ectodysplasin pathway: from diseases to adaptations

(2013) Alexa Sadier et al.   TRENDS IN GENETICS

Genetic basis of dental agenesis - molecular genetics patterning clinical dentistry

(2013) N. Chhabra et al.   Medicina Oral Patologia Oral y Cirugia Bucal

Mutations inWNT10Aare present in more than half of isolated hypodontia cases

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

AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome

(2011) Monica L. Marvin 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

Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A

(2011) Gabriela Petrof et al.   AUSTRALASIAN JOURNAL OF DERMATOLOGY

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 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

Genetic basis of tooth agenesis

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

Protein structure prediction on the Web: a case study using the Phyre server

(2009) Lawrence A Kelley et al.   Nature Protocols

Polymorphism in the Msx1 gene associated with hypodontia in a Brazilian family

(2009) Elisângela R. Silva et al.   Journal of Oral Science

Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis

(2008) N. Callahan et al.   ARCHIVES OF ORAL BIOLOGY

Identification and Functional Analysis of Two Novel PAX9 Mutations

(2008) Ying Wang et al.   CELLS TISSUES ORGANS

Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis

(2008) Dong Han et al.   European Journal of Medical Genetics

PAX9 polymorphisms and susceptibility to sporadic tooth agenesis: a case–control study in southeast China

(2008) Yongchu Pan et al.   EUROPEAN JOURNAL OF ORAL SCIENCES