WNT10Amutations also associated with agenesis of the maxillary permanent canines, a separate entity-Reference-Cited by-同舟云学术

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

Published:2013-12-05 Issue:2 Volume:164 Page:360-363
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Kantaputra P.¹²³,Kaewgahya M.²,Kantaputra W.²³

Affiliation:

1. Division of Pediatric Dentistry; Department of Orthodontics and Pediatric Dentistry; Faculty of Dentistry; Chiang Mai University; Chiang Mai Thailand

2. Craniofacial Genetics Laboratory; Faculty of Dentistry; Chiang Mai University; Chiang Mai Thailand

3. Dentaland Clinic; Chiang Mai Thailand

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36280/fullpdf

Reference22 articles.

1. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: The odonto-onycho-dermal dysplasia;Adaimy;Am J Hum Genet,2007

2. Deciduous dentition of the aye aye, Daubentonia madagascariensis;Ankel-Simons;Am J Primatol,1996

3. A congenitally missing canine in association with other dental disturbances: Report of two cases;Bazan;ASDC J Dent Child,1983

4. WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes;Bohring;Am J Hum Genet,2009

5. Congenitally missing maxillary permanent canines: Report of 32 cases from an ethnic Chinese population;Cho;Int J Paediatr Dent,2004

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