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WNT10A and isolated hypodontia.
Am J Med Genet A. 2011 May; 155A(5):1119-22.AJ

Abstract

WNT10A has been associated with various syndromes with ectodermal dysplasia from severe autosomal recessive SchO?pf-Schulz-Passarge syndrome to odonto-onycho-dermal dysplasia and autosomal dominant hypodontia. We report WNT10A mutations in an American family of which four members are affected with isolated hypodontia or microdontia. Here we demonstrate that in addition to MSX1, PAX9, AXIN2, and EDA, mutations in WNT10A can cause isolated hypodontia.

Authors+Show Affiliations

Division of Pediatric Dentistry, Department of Orthodontics and Pediatric Dentistry, Faculty of Dentistry, Craniofacial Genetics Laboratory, Chiang Mai University, Thailand. dentaland17@gmail.comNo affiliation info available

Pub Type(s)

Case Reports
Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

21484994

Citation

Kantaputra, Piranit, and Warissara Sripathomsawat. "WNT10A and Isolated Hypodontia." American Journal of Medical Genetics. Part A, vol. 155A, no. 5, 2011, pp. 1119-22.
Kantaputra P, Sripathomsawat W. WNT10A and isolated hypodontia. Am J Med Genet A. 2011;155A(5):1119-22.
Kantaputra, P., & Sripathomsawat, W. (2011). WNT10A and isolated hypodontia. American Journal of Medical Genetics. Part A, 155A(5), 1119-22. https://doi.org/10.1002/ajmg.a.33840
Kantaputra P, Sripathomsawat W. WNT10A and Isolated Hypodontia. Am J Med Genet A. 2011;155A(5):1119-22. PubMed PMID: 21484994.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - WNT10A and isolated hypodontia. AU - Kantaputra,Piranit, AU - Sripathomsawat,Warissara, Y1 - 2011/04/11/ PY - 2010/10/05/received PY - 2010/11/04/accepted PY - 2011/4/13/entrez PY - 2011/4/13/pubmed PY - 2011/8/2/medline SP - 1119 EP - 22 JF - American journal of medical genetics. Part A JO - Am J Med Genet A VL - 155A IS - 5 N2 - WNT10A has been associated with various syndromes with ectodermal dysplasia from severe autosomal recessive SchO?pf-Schulz-Passarge syndrome to odonto-onycho-dermal dysplasia and autosomal dominant hypodontia. We report WNT10A mutations in an American family of which four members are affected with isolated hypodontia or microdontia. Here we demonstrate that in addition to MSX1, PAX9, AXIN2, and EDA, mutations in WNT10A can cause isolated hypodontia. SN - 1552-4833 UR - https://wwww.unboundmedicine.com/medline/citation/21484994/WNT10A_and_isolated_hypodontia_ L2 - https://doi.org/10.1002/ajmg.a.33840 DB - PRIME DP - Unbound Medicine ER -
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