One gene, two phenotypes:ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B-Reference-Cited by-同舟云学术

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One gene, two phenotypes:ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B

Published:2003-06-13 Issue:1 Volume:22 Page:1-11
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Afzal Ali R.,Jeffery Steve

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference92 articles.

1. Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22

2. Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2

3. Congenital heart disease in Robinow syndrome

4. Expression of the Ror1 and Ror2 receptor tyrosine kinase genes during mouse development

5. Recommendations for a nomenclature system for human gene mutations

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