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dc.contributor.authorCanatan, D.
dc.contributor.authorBilgen, Türker
dc.contributor.authorÇiftçi, V.
dc.contributor.authorYazıcı, G.
dc.contributor.authorDelibaş, S.
dc.contributor.authorKeser, İ.
dc.date.accessioned2022-05-11T14:48:08Z
dc.date.available2022-05-11T14:48:08Z
dc.date.issued2016
dc.identifier.issn1300-7777
dc.identifier.urihttps://doi.org/10.4274/tjh.2015.0299
dc.identifier.urihttps://hdl.handle.net/20.500.11776/10604
dc.description.abstract[No abstract available]en_US
dc.language.isoengen_US
dc.publisherTurkish Society of Hematologyen_US
dc.identifier.doi10.4274/tjh.2015.0299
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAbnormal hemoglobinsen_US
dc.subjectHemoglobin fontainebleauen_US
dc.subjectHemoglobin G-Waimanaloen_US
dc.subjectDNAen_US
dc.subjecthemoglobin beta chainen_US
dc.subjecthemoglobin fontainebleauen_US
dc.subjecthemoglobin g Waimanaloen_US
dc.subjecthemoglobin varianten_US
dc.subjectunclassified drugen_US
dc.subjectcodonen_US
dc.subjecthemoglobin alpha chainen_US
dc.subjecthemoglobin Fontainebleauen_US
dc.subjecthemoglobin G Waimanaloen_US
dc.subjecthemoglobin varianten_US
dc.subjectadulten_US
dc.subjectalpha gene A1en_US
dc.subjectalpha gene A2en_US
dc.subjectblood analysisen_US
dc.subjectblood cell counten_US
dc.subjectcase reporten_US
dc.subjectDNA sequenceen_US
dc.subjectfemaleen_US
dc.subjectgeneen_US
dc.subjectgene mutationen_US
dc.subjecthematologic diseaseen_US
dc.subjecthigh performance liquid chromatographyen_US
dc.subjecthumanen_US
dc.subjectLetteren_US
dc.subjectnormochromic normocytic anemiaen_US
dc.subjectpolymerase chain reactionen_US
dc.subjectthalassemiaen_US
dc.subjectTurk (people)en_US
dc.subjectalpha-Thalassemiaen_US
dc.subjectasymptomatic diseaseen_US
dc.subjectcodonen_US
dc.subjectgeneticsen_US
dc.subjectmissense mutationen_US
dc.subjectpoint mutationen_US
dc.subjectTurkeyen_US
dc.subjectAdulten_US
dc.subjectalpha-Globinsen_US
dc.subjectalpha-Thalassemiaen_US
dc.subjectAsymptomatic Diseasesen_US
dc.subjectChromatography, High Pressure Liquiden_US
dc.subjectCodonen_US
dc.subjectFemaleen_US
dc.subjectHemoglobins, Abnormalen_US
dc.subjectHumansen_US
dc.subjectMutation, Missenseen_US
dc.subjectPoint Mutationen_US
dc.subjectTurkeyen_US
dc.titleFirst observation of hemoglobin G-waimanalo and hemoglobin fontainebleau cases in the Turkish populationen_US
dc.title.alternativeTürk toplumunda gözlenen ilk hemoglobin g-waimanalo ve hemoglobin fontainebleau olguları]en_US
dc.typeletteren_US
dc.relation.ispartofTurkish Journal of Hematologyen_US
dc.departmentRektörlüğe Bağlı Bölümler, Rektörlük, Bilimsel ve Teknolojik Araştırmalar Uygulama ve Araştırma Merkezien_US
dc.identifier.volume33en_US
dc.identifier.issue1en_US
dc.identifier.startpage71en_US
dc.identifier.endpage72en_US
dc.institutionauthorBilgen, Türker
dc.relation.publicationcategoryDiğeren_US
dc.authorscopusid6701448163
dc.authorscopusid9242258800
dc.authorscopusid57130822200
dc.authorscopusid57130497800
dc.authorscopusid57130808000
dc.authorscopusid6701531346
dc.identifier.scopus2-s2.0-84958787178en_US
dc.identifier.pmid27020723en_US


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