1: Patton MA, Afzal AR. Related Articles, Links
Robinow syndrome.
J Med Genet. 2002 May;39(5):305-10. Review.
PMID: 12011143 [PubMed - indexed for MEDLINE]
2: Kantaputra PN, Kinoshita A, Limwonges C, Praditsup O, Niikawa N. Related Articles, Links
A Thai mother and son with distal symphalangism, hypoplastic carpal bones, microdontia, dental pulp stones, and narrowing of the zygomatic arch: a new distal symphalangism syndrome?
Am J Med Genet. 2002 Apr 15;109(1):56-60.
PMID: 11932993 [PubMed - indexed for MEDLINE]
3: 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]
4: 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]
5: Afzal AR, Rajab A, Fenske CD, Oldridge M, Elanko N, Ternes-Pereira E, Tuysuz B, Murday VA, Patton MA, Wilkie AO, Jeffery S. Related Articles, Links
Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2.
Nat Genet. 2000 Aug;25(4):419-22.
PMID: 10932186 [PubMed - indexed for MEDLINE]
Time used: 16 miliseconds.

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