OMIM/113000[Secondary Source ID] - Search Results

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

Bacchelli C, Wilson LC, Cook JA, Winter RM, Goodman FR. Bacchelli C, et al. Clin Genet. 2003 Sep;64(3):263-5. doi: 10.1034/j.1399-0004.2003.00139.x. Clin Genet. 2003. PMID: 12919145 No abstract available.

Expression of the Ror1 and Ror2 receptor tyrosine kinase genes during mouse development.

Al-Shawi R, Ashton SV, Underwood C, Simons JP. Al-Shawi R, et al. Dev Genes Evol. 2001 Apr;211(4):161-71. doi: 10.1007/s004270100140. Dev Genes Evol. 2001. PMID: 11455430

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