WNT10Amutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations
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Title
WNT10Amutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations
Authors
Keywords
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Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume 164, Issue 2, Pages 353-359
Publisher
Wiley
Online
2013-11-26
DOI
10.1002/ajmg.a.36243
References
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Related references
Note: Only part of the references are listed.- 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
- Tooth shape formation and tooth renewal: evolving with the same signals
- (2012) J. Jernvall et al. DEVELOPMENT
- 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
- 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
- Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation, p.Cys107X, in WNT10A
- (2011) Gabriela Petrof et al. AUSTRALASIAN JOURNAL OF DERMATOLOGY
- Phenotypic variability associated with WNT10A nonsense mutations
- (2010) M. Van Geel et al. BRITISH JOURNAL OF DERMATOLOGY
- Wnt/β-catenin Signaling in Oral Tissue Development and Disease
- (2010) F. Liu et al. JOURNAL OF DENTAL RESEARCH
- 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
- Classifying ectodermal dysplasias: Incorporating the molecular basis and pathways (Workshop II)
- (2009) J. Timothy Wright et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Ectodermal dysplasias: Clinical and molecular review
- (2009) Átila F. Visinoni et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- WNT10A missense mutation associated with a complete Odonto-Onycho-Dermal Dysplasia syndrome
- (2009) Sadia Nawaz et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Genetic basis of tooth agenesis
- (2009) Pekka Nieminen JOURNAL OF EXPERIMENTAL ZOOLOGY PART B-MOLECULAR AND DEVELOPMENTAL EVOLUTION
- An Ancient Gene Network Is Co-opted for Teeth on Old and New Jaws
- (2009) Gareth J Fraser et al. PLOS BIOLOGY
- Wnt/β-catenin signaling directs multiple stages of tooth morphogenesis
- (2007) Fei Liu et al. DEVELOPMENTAL BIOLOGY
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