Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia-Reference-Cited by-同舟云学术

Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia

Published:2003-02 Issue:2 Volume:72 Page:408-418
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Paznekas William A.,Boyadjiev Simeon A.,Shapiro Robert E.,Daniels Otto,Wollnik Bernd,Keegan Catherine E.,Innis Jeffrey W.,Dinulos Mary Beth,Christian Cathy,Hannibal Mark C.,Jabs Ethylin Wang

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference62 articles.

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3. Boyadjiev SA, Chowdry AB, Shapiro RE, Paznekas WA, Wandstrat AE, Choi JW, Kasch L, Zhang G, Wollnik B, Burgess CE, Schalling M, Lovett M, Jabs EW. Physical map of the chromosome 6q22 region containing the oculodentodigital dysplasia locus: analysis of thirteen candidate genes and identification of novel ESTs and DNA polymorphisms. Cytogenet Genome Res (in press).

4. Mutations of the connexin43 gap-junction gene in patients with heart malformations and defects of laterality;Britz-Cunningham;N Engl J Med,1995

5. Connexin 43 mediates direct intercellular communication in human osteoblastic cell networks;Civitelli;J Clin Invest,1993

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