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DNA ANALYSIS IN TURKISH DUCHENNE BECKER MUSCULAR-DYSTROPHY FAMILIES

dc.contributor.authorKUSEYRI, F
dc.contributor.authorTELATAR, M
dc.contributor.authorDEYMEER, F
dc.contributor.authorSERDAROGLU, P
dc.contributor.authorTOLUN, A
dc.contributor.authorAPAK, M
dc.contributor.authorOZDEMIR, C
dc.contributor.authorBATTALOGLU, E
dc.date.accessioned2021-03-04T11:08:57Z
dc.date.available2021-03-04T11:08:57Z
dc.date.issued1992
dc.identifier.citationBATTALOGLU E., TELATAR M., DEYMEER F., SERDAROGLU P., KUSEYRI F., OZDEMIR C., APAK M., TOLUN A., "DNA ANALYSIS IN TURKISH DUCHENNE BECKER MUSCULAR-DYSTROPHY FAMILIES", HUMAN GENETICS, cilt.89, sa.6, ss.635-639, 1992
dc.identifier.issn0340-6717
dc.identifier.otherav_70d233ca-47e6-494b-8df6-49ee2d28a5e6
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/77760
dc.identifier.urihttps://doi.org/10.1007/bf00221954
dc.description.abstractThe molecular genetics of Duchenne/Becker muscular dystrophy was investigated in 81 affected Turkish families. Deletions were detected by multiplex polymerase chain reaction assays and cDNA Southern analyses. The distribution of the deletions along the gene and their correlation to clinical phenotype were different from the studies reported on other populations. Moreover, DNA polymorphisms in mothers were determined using 8 DNA probes and three CA repeat sequences, and a high degree of informativeness was observed.
dc.language.isoeng
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectGENETİK VE HAYAT
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.titleDNA ANALYSIS IN TURKISH DUCHENNE BECKER MUSCULAR-DYSTROPHY FAMILIES
dc.typeMakale
dc.relation.journalHUMAN GENETICS
dc.contributor.department, ,
dc.identifier.volume89
dc.identifier.issue6
dc.identifier.startpage635
dc.identifier.endpage639
dc.contributor.firstauthorID113722


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