Literature DB >> 10710232

Anodontia of permanent teeth (OMIM # 206780) and pegged/missing maxillary lateral incisors (OMIM # 150400) in the same family.

J J Hoo.   

Abstract

Mesh：

Year:  2000        PMID： 10710232     DOI： 10.1002/(sici)1096-8628(20000214)90:4<326::aid-ajmg12>3.0.co;2-o

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  2 in total

1.  WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

Authors:  Axel Bohring; Thomas Stamm; Christiane Spaich; Claudia Haase; Kerstin Spree; Ute Hehr; Mandy Hoffmann; Susanne Ledig; Saadettin Sel; Peter Wieacker; Albrecht Röpke
Journal:  Am J Hum Genet       Date:  2009-06-25       Impact factor: 11.025

2.  PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China.

Authors:  Jing Wang; Yuanzhi Xu; Jing Chen; Feiyu Wang; Renhuan Huang; Songtao Wu; Linjing Shu; Jingyi Qiu; Zhi Yang; Junjie Xue; Raorao Wang; Jilin Zhao; Wenli Lai
Journal:  J Appl Oral Sci       Date:  2013       Impact factor: 2.698
  2 in total

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