Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta-Reference-Cited by-同舟云学术

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Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta

Published:2004-07-01 Issue:7 Volume:41 Page:545-549
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Hart P S

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Cited by 226 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. Roles of the histone methyltransferase SET domain bifurcated 1 in epithelial cells during tooth development;Archives of Oral Biology;2024-09

2. Investigating the impact of kallikrein 4 gene polymorphism on caries severity and development in divers age groups of pregnant women during caries prevention;Pediatric dentistry and dental prophylaxis;2024-01-22

3. A novel ODAPH mutation causing amelogenesis imperfecta and its expression in human dental tissues;Journal of Dental Sciences;2024-01

4. Digenic inheritance accounts for phenotypic variability in amelogenesis imperfecta;Clinical Genetics;2023-11-08

5. Role of Genetic Markers in Dental Caries: A Literature Review;Journal of Health and Allied Sciences NU;2023-07-31

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