Inhabitual autosomal recessive form of dentin dysplasia type I in a large consanguineous Moroccan family-Reference-Cited by-同舟云学术

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Inhabitual autosomal recessive form of dentin dysplasia type I in a large consanguineous Moroccan family

Published:2013-08 Issue:8 Volume:56 Page:442-444
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Cherkaoui Jaouad I.,El Alloussi M.,Laarabi F.Z.,Bouhouche A.,Ameziane R.,Sefiani A.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference14 articles.

1. Hereditary dentin defects;Kim;J. Dent Res.,2007

2. A proposed classification for heritable human dentine defects with a description of a new entity;Shields;Arch. Oral Biol.,1973

3. Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP;Xiao;Nat. Genet.,2001

4. DSPP mutation in dentinogenesis imperfecta Shields type II;Zhang;Nat. Genet.,2001

5. A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II;Kim;Hum. Genet.,2004

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1. Developmental Defects of the Teeth and Their Hard Tissues;Pediatric Dentistry;2022

2. A case of multiple rootless teeth: A case report and review;Journal of Oral and Maxillofacial Pathology;2021

3. Endodontic treatment of dentin dysplasia type I D;Australian Endodontic Journal;2020-09-22

4. Dentin dysplasia type I;Folia Morphologica;2019-08-29

5. Vps4b heterozygous mice do not develop tooth defects that replicate human dentin dysplasia I;BMC Genetics;2019-01-11

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