Enamelin/ameloblastin gene polymorphisms in autosomal amelogenesis imperfecta among Syrian families
Author:
Publisher
Wiley
Subject
General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.2041-1626.2010.00038.x/fullpdf
Reference22 articles.
1. Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary;Kida;J Dent Res,2002
2. X-linked amelogenesis imperfecta. Presentation of two kindreds and a review of the literature;Crawford;Oral Surg Oral Med Oral Pathol,1992
3. Amelogenesis imperfecta Orphanet;Crawford;J Rare Dis,2007
4. Amelogenesis imperfecta: a genetic study;Backman;Hum Hered,1988
5. The genetics of amelogenesis imperfecta. A review of the literature;Santos;J Appl Oral Sci,2005
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1. Etiological Exploration of Enamel Defects: A cross-sectional study to Unravel Maternal, Prenatal, and Early Childhood Influences;2024-04-04
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3. An ameloblastin C-terminus variant is present in human adipose tissue;Heliyon;2018-12
4. JICD matters;Journal of Investigative and Clinical Dentistry;2011-02
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