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Autosomal recessive Robinow syndrome is allelic to dominant brachydactyly type B and caused by loss of function mutations in ROR2

dc.contributor.authorTuysuz, B
dc.contributor.authorFenske, CD
dc.contributor.authorOldridge, M
dc.contributor.authorElanko, N
dc.contributor.authorTernes-Pereira, E
dc.contributor.authorWilkie, AOM
dc.contributor.authorPatton, MA
dc.contributor.authorMurday, VA
dc.contributor.authorJeffrey, S
dc.contributor.authorAfzal, AR
dc.contributor.authorRajab, A
dc.date.accessioned2021-03-04T07:59:39Z
dc.date.available2021-03-04T07:59:39Z
dc.identifier.citationAfzal A., Rajab A., Fenske C., Oldridge M., Elanko N., Ternes-Pereira E., Tuysuz B., Murday V., Patton M., Wilkie A., et al., "Autosomal recessive Robinow syndrome is allelic to dominant brachydactyly type B and caused by loss of function mutations in ROR2", JOURNAL OF MEDICAL GENETICS, cilt.37, 2000
dc.identifier.issn0022-2593
dc.identifier.othervv_1032021
dc.identifier.otherav_60fd25dd-6464-438a-8f44-ee8617ecb8f9
dc.identifier.urihttp://hdl.handle.net/20.500.12627/67652
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titleAutosomal recessive Robinow syndrome is allelic to dominant brachydactyly type B and caused by loss of function mutations in ROR2
dc.typeMakale
dc.relation.journalJOURNAL OF MEDICAL GENETICS
dc.contributor.department, ,
dc.identifier.volume37
dc.contributor.firstauthorID126428


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