Candidate-gene exclusion in a family with inherited non-syndromic dental disorders-Reference-Cited by-同舟云学术

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Candidate-gene exclusion in a family with inherited non-syndromic dental disorders

Published:2012-12 Issue:2 Volume:511 Page:420-426
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Li Li,Shu Yi,Lou Beiyan,Wu Hongkun

Funder

Department of Geriatric Dentistry, of West China College of Stomatology, Sichuan University.

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference36 articles.

1. Phenotype characterization and DSPP mutational analysis of three Brazilian dentinogenesis imperfecta type II families;Acevedo;Cells Tissues Organs,2009

2. Amelogenesis imperfecta — clinical manifestations in 51 families in a northern Swedish county;Bäckman;Scand. J. Dent. Res.,1988

3. The genetic basis of inherited anomalies of the teeth. Part 1: clinical and molecular aspects of non-syndromic dental disorders;Bailleul-Forestier;Eur. J. Med. Genet.,2008

4. Clinical features of a family with X-linked amelogenesis imperfecta mapping to a new locus (AIH3) on the long arm of the X chromosome;Crawford;Oral Surg. Oral Med. Oral Pathol.,1993

5. Mapping of the human tuftelin (TUFT1) gene to Chromosome 1 by fluorescence in situ hybridization

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Symmetric multiquadrant isolated dentin dysplasia (SMIDD), a unique presentation mimicking dentin dysplasia type 1b;Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology;2017-05

2. Deletion of ameloblastin exon 6 is associated with amelogenesis imperfecta;Human Molecular Genetics;2014-05-23

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