Relationship of Phenotype and Genotype in X-Linked Amelogenesis Imperfecta-Reference-Cited by-同舟云学术

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Relationship of Phenotype and Genotype in X-Linked Amelogenesis Imperfecta

Published:2003-01 Issue:1 Volume:44 Page:72-78
ISSN:0300-8207
Container-title:Connective Tissue Research
language:en
Short-container-title:Connective Tissue Research

Author:

Wright J. T.,Hart P. S.,Aldred M. J.,Seow K.,Crawford P. J. M.,Hong S. P.,Gibson C. W.,Hart T. C.

Publisher

Informa UK Limited

Subject

Cell Biology,Molecular Biology,Orthopedics and Sports Medicine,Biochemistry,Rheumatology

Link

http://www.tandfonline.com/doi/pdf/10.1080/03008200390152124

Reference40 articles.

1. Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification

2. Mutational analysis of X-linked amelogenesis imperfecta in multiple families

3. Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta

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3. Resolving protein-mineral interfacial interactions during in vitro mineralization by atom probe tomography;Materials Today Advances;2023-06

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5. Novel WDR72 Mutations Causing Hypomaturation Amelogenesis Imperfecta;Journal of Personalized Medicine;2023-02-14

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