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PMID: 14729836 Published · ppublish English Letter Multicenter Study Research Support, Non-U.S. Gov't

Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly.

Journal of medical genetics ·Vol. 41 ·No. 1 ·2004-01-00 ·Pages 60-7

Richardson R, Donnai D, Meire F, Dixon MJ

Abstract

暂无摘要

MeSH Terms
Abnormalities, Multiple/genetics Amino Acid Sequence/genetics Animals Cattle Connexin 43/chemistry,genetics,physiology Craniofacial Abnormalities/genetics Cricetinae Embryo, Mammalian/chemistry,metabolism Eye Abnormalities/genetics Fingers/abnormalities Gene Expression Regulation, Developmental/genetics,physiology Humans Mice Molecular Sequence Data Mutation, Missense/genetics Phenotype Rats Sequence Alignment Syndactyly/genetics Syndrome Tooth Abnormalities/genetics
Chemicals
Connexin 43
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Richardson R
Donnai D
Meire F
Dixon M J
Article Info
Journal
Journal of medical genetics
Abbr.
J Med Genet
ISSN
1468-6244
Published
2004-01-00
Pages
60-7
Language
English
Region
England
NLM ID
2985087R
PMCID
PMC1757241
Subset
IM
Databases
OMIM
164200
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