Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III-Reference-Cited by-同舟云学术

Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III

Published:2004-12-16 Issue:3 Volume:132A Page:305-309
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Dong Juan,Gu TingTing,Jeffords Leticia,MacDougall Mary

Funder

National Institute of Dental and Craniofacial Research, National Institute of Health

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference20 articles.

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2. An autosomal-dominant form of juvenile periodontitis: Its localization to chromosome 4 and linkage to dentinogenesis imperfecta and Gc;Boughman;J Craniofac Genet Dev Biol,1986

3. Trinucleotide repeats: Mechanisms and pathophysiology;Cummings;Annu Rev Genomics Hum Genet,2000

4. Gene expression patterns of murine dentin matrix protein 1 (Dmp1) and dentin sialophosphoprotein (DSPP) suggest distinct developmental functions in vivo;D'Souza;J Bone Miner Res,1997

5. Genetic linkage of dentin dysplasia type II to chromosome 4q;Dean;J Craniofac Genet Dev Biol,1997

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