Quiz in hematology diagnosis : congenital dyserythropoietic anemia type 2 due to compound heterozygote mutation in SEC23B gene
dc.authorid | 0000-0003-2469-9509 | en_US |
dc.contributor.author | Demircioğlu, Fatih | |
dc.contributor.author | Erkoçoğlu, Mustafa | |
dc.contributor.author | Dilek, Mustafa | |
dc.contributor.author | Bekdaş, Mervan | |
dc.contributor.author | Göksügür, Sevil Bilir | |
dc.contributor.author | Büyükkorkmaz, Semra | |
dc.contributor.author | Açar, Seher | |
dc.date.accessioned | 2021-06-23T19:41:56Z | |
dc.date.available | 2021-06-23T19:41:56Z | |
dc.date.issued | 2015 | |
dc.department | BAİBÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü | en_US |
dc.identifier.doi | 10.4274/tjh.2014.0478 | |
dc.identifier.endpage | 284 | en_US |
dc.identifier.issn | 1300-7777 | |
dc.identifier.issn | 1308-5263 | |
dc.identifier.issue | 3 | en_US |
dc.identifier.pmid | 25912935 | en_US |
dc.identifier.scopus | 2-s2.0-84938541056 | en_US |
dc.identifier.scopusquality | Q3 | en_US |
dc.identifier.startpage | 283 | en_US |
dc.identifier.uri | https://doi.org/10.4274/tjh.2014.0478 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12491/8242 | |
dc.identifier.volume | 32 | en_US |
dc.identifier.wos | WOS:000363092000018 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.institutionauthor | Demircioğlu, Fatih | |
dc.institutionauthor | Erkoçoğlu, Mustafa | |
dc.institutionauthor | Dilek, Mustafa | |
dc.institutionauthor | Bekdaş, Mervan | |
dc.institutionauthor | Göksügür, Sevil Bilir | |
dc.institutionauthor | Büyükkorkmaz, Semra | |
dc.institutionauthor | Açar, Seher | |
dc.language.iso | en | en_US |
dc.publisher | Galenos Yayıncılık | en_US |
dc.relation.ispartof | Turkish Journal Of Hematology | en_US |
dc.relation.publicationcategory | Diğer | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Anemia | en_US |
dc.subject | Congenital Dyserythropoietic Anemia Type 2 | en_US |
dc.subject | SEC23B Gene | en_US |
dc.title | Quiz in hematology diagnosis : congenital dyserythropoietic anemia type 2 due to compound heterozygote mutation in SEC23B gene | en_US |
dc.type | Editorial | en_US |
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