Associated Papers
A novel variant in the ROR2 gene underlying brachydactyly type B: a case report.
Shao J et al.
Bmc Pediatrics, 2022
A homozygous ROR2 variant in a family with atypical Robinow syndrome and tetramelic transverse deficiency of autopods.
Malik S et al.
American Journal of Medical Genetics. Part A, 2022
A new mutation in the gene ROR2 causes brachydactyly type B1.
Huang D et al.
Gene, 2014
A systematic review of genetic skeletal disorders reported in Chinese biomedical journals between 1978 and 2012.
Cui Y et al.
Orphanet Journal of Rare Diseases, 2012
[Mutation analysis of the pathogenic gene in a Chinese family with Brachydactyly type B1].
Li CM et al.
Yi Chuan = Hereditas, 2011
PhenoHM: human-mouse comparative phenome-genome server.
Sardana D et al.
Nucleic Acids Research, 2010
20507906 (PubMed )
Supplement: gkq472_nar-00429-web-b-2010-File006.xls › MPO_to_OMIM_allelic_Variants
A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese family.
Lv D et al.
Journal of Human Genetics, 2009
Dominant versus recessive traits conveyed by allelic mutations - to what extent is nonsense-mediated decay involved?
Ben-Shachar S et al.
Clinical Genetics, 2009
The deleted in brachydactyly B domain of ROR2 is required for receptor activation by recruitment of Src.
Akbarzadeh S et al.
Plos One, 2008
Brachydactyly type B1: report of a family with de novo ROR2 mutation.
Hamamy H et al.
Clinical Genetics, 2006
[Genetic analysis of the UGT1A1 gene mutation sites in a Chinese family suffered from Gilbert's syndrome].
Yu LH et al.
Yi Chuan = Hereditas, 2006
[Identification of a recurrent mutation in the ROR2 gene in a Chinese family with brachydactyly type B].
Yang W et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2004
One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B.
Afzal AR et al.
Human Mutation, 2003
Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B.
Schwabe GC et al.
American Journal of Human Genetics, 2000
Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B.
Oldridge M et al.
Nature Genetics, 2000
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