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dc.contributor.authorHART, TC
dc.contributor.authorÖzdemir, D
dc.contributor.authorUygur, C
dc.contributor.authorRyu, OK
dc.contributor.authorMikhalek, MD
dc.contributor.authorGorry, MC
dc.contributor.authorHART, PS
dc.contributor.authorAREN, GAMZE
dc.contributor.authorFIRATLI, HALIL ERHAN
dc.contributor.authorFIRATLI, SÖNMEZ
dc.date.accessioned2021-03-04T11:17:29Z
dc.date.available2021-03-04T11:17:29Z
dc.identifier.citationHART T., HART P., Gorry M., Mikhalek M., Ryu O., Uygur C., Özdemir D., FIRATLI S., AREN G., FIRATLI H. E. , "Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localized enamel defects.", Annual Meeting of the American-Society-of-Human-Genetics, Amerika Birleşik Devletleri, 1 - 04 Kasım 2003, cilt.73, sa.5, ss.558
dc.identifier.otherav_71937212-f0d6-4d89-b8c0-0c02dc9f55c0
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/78210
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri
dc.titleNovel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localized enamel defects.
dc.typeBildiri
dc.contributor.department, ,
dc.identifier.volume73
dc.contributor.firstauthorID396156


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