1: Schwabe GC, Tinschert S, Buschow C, Meinecke P, Wolff G, Gillessen-Kaesbach G, Oldridge M, Wilkie AO, Komec R, Mundlos S. Related Articles, Links
Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B.
Am J Hum Genet. 2000 Oct;67(4):822-31.
PMID: 10986040 [PubMed - indexed for MEDLINE]
2: van Bokhoven H, Celli J, Kayserili H, van Beusekom E, Balci S, Brussel W, Skovby F, Kerr B, Percin EF, Akarsu N, Brunner HG. Related Articles, Links
Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome.
Nat Genet. 2000 Aug;25(4):423-6.
PMID: 10932187 [PubMed - indexed for MEDLINE]
3: Oldridge M, Fortuna AM, Maringa M, Propping P, Mansour S, Pollitt C, DeChiara TM, Kimble RB, Valenzuela DM, Yancopoulos GD, Wilkie AO. Related Articles, Links
Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B.
Nat Genet. 2000 Mar;24(3):275-8.
PMID: 10700182 [PubMed - indexed for MEDLINE]
4: DeChiara TM, Kimble RB, Poueymirou WT, Rojas J, Masiakowski P, Valenzuela DM, Yancopoulos GD. Related Articles, Links
Ror2, encoding a receptor-like tyrosine kinase, is required for cartilage and growth plate development.
Nat Genet. 2000 Mar;24(3):271-4.
PMID: 10700181 [PubMed - indexed for MEDLINE]
5: Oishi I, Takeuchi S, Hashimoto R, Nagabukuro A, Ueda T, Liu ZJ, Hatta T, Akira S, Matsuda Y, Yamamura H, Otani H, Minami Y. Related Articles, Links
Spatio-temporally regulated expression of receptor tyrosine kinases, mRor1, mRor2, during mouse development: implications in development and function of the nervous system.
Genes Cells. 1999 Jan;4(1):41-56.
PMID: 10231392 [PubMed - indexed for MEDLINE]
Time used: 31 miliseconds.

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