Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2-Reference-Cited by-同舟云学术

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

Published:2000-08 Issue:4 Volume:25 Page:419-422
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Afzal Ali R.,Rajab Anna,Fenske Christiane D.,Oldridge Michael,Elanko Navaratnam,Ternes-Pereira Eliana,Tüysüz Beyhan,Murday Victoria A.,Patton Michael A.,Wilkie Andrew O.M.,Jeffery Steve

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0800_419.pdf

Reference30 articles.

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2. Soliman, A.T, Rajab, A., Alsalmi, I. & Aziz Bedair, S.M. Recessive Robinow syndrome: with emphasis on endocrine functions. Metabolism 47, 1337–1343 (1998).

3. Wadia, R.S. Recessively inherited costovertebral segmentation defect with mesomelia and peculiar facies (Covesdem syndrome): a new genetic entity? J. Med. Genet. 15, 123–127 (1978).

4. Afzal, A.R. et al. Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22. Hum. Genet. 106, 351–354 (2000).

5. Gong, Y. et al. Brachydactyly type B: clinical description, genetic mapping to chromosome 9q and evidence for a shared ancestral mutation. Am. J. Hum. Genet. 64, 570–577 (1999).

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