(Q28245887)

2

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Wei Yang

3

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Lihua Cao

4

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Yaran Wen

5

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Xiuli Zhao

6

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Miao Sun

7

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Wilson H-Y Lo

8

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Xue Zhang

Journal of Human Genetics

9

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language of work or name

English

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publication date

July 2009

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published in

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volume

54

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issue

7

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page(s)

422-5

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cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.48

7 January 2021

Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.48

7 January 2021

Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.48

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.48

7 January 2021

Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.48

7 January 2021

ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.48

7 January 2021

Brachydactyly type B1: report of a family with de novo ROR2 mutation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.48

7 January 2021

Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.48

7 January 2021

Localization of a gene for syndactyly type 1 to chromosome 2q34-q36.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.48

7 January 2021

Confirmation of genetic homogeneity of syndactyly type 1 in an Iranian family

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.48

7 January 2021

Dominant versus recessive traits conveyed by allelic mutations - to what extent is nonsense-mediated decay involved?

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.48

7 January 2021

A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.48

7 January 2021