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dc.contributor.authorÖzdemir, D
dc.contributor.authorAREN, Gamze
dc.contributor.authorUygur, C
dc.contributor.authorFiratli, Sönmez
dc.contributor.authorFIRATLI, E
dc.contributor.authorHART, TC
dc.contributor.authorHART, PS
dc.contributor.authorGorry, MC
dc.contributor.authorMICHALEC, MD
dc.contributor.authorRYU, O
dc.date.accessioned2021-03-03T21:11:00Z
dc.date.available2021-03-03T21:11:00Z
dc.identifier.citationHART T., HART P., Gorry M., MICHALEC M., RYU O., Uygur C., Özdemir D., Firatli S., AREN G., FIRATLI E., "Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localized enamel defects.", Annual Meeting of the American-Society-of-Human-Genetics, Los-Angeles, Şili, 4 - 08 Kasım 2003, cilt.73, ss.558
dc.identifier.othervv_1032021
dc.identifier.otherav_5dda5ff6-e491-4863-a517-009a172f4739
dc.identifier.urihttp://hdl.handle.net/20.500.12627/65670
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.subjectTıp
dc.titleNovel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localized enamel defects.
dc.typeBildiri
dc.contributor.department, ,
dc.identifier.volume73
dc.contributor.firstauthorID86065


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