Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome-Reference-Cited by-同舟云学术

Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome

Published:2015-04 Issue:4 Volume:96 Page:623-630
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Bunn Kieran J.,Daniel Phil,Rösken Heleen S.,O’Neill Adam C.,Cameron-Christie Sophia R.,Morgan Tim,Brunner Han G.,Lai Angeline,Kunst Henricus P.M.,Markie David M.,Robertson Stephen P.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference48 articles.

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2. Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2;Afzal;Nat. Genet.,2000

3. Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome;van Bokhoven;Nat. Genet.,2000

4. WNT5A mutations in patients with autosomal dominant Robinow syndrome;Person;Dev. Dyn.,2010

5. The complex world of WNT receptor signalling;Niehrs;Nat. Rev. Mol. Cell Biol.,2012

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