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dc.contributor.authorAydogan, G.
dc.contributor.authorGulec, E. Yilmaz
dc.contributor.authorSalcioglu, Z.
dc.contributor.authorAkici, F.
dc.contributor.authorKeskindemirci, Gonca
dc.contributor.authorTugcu, Deniz
dc.contributor.authorBartsch, O.
dc.contributor.authorBayram, C.
dc.date.accessioned2021-03-05T13:33:51Z
dc.date.available2021-03-05T13:33:51Z
dc.identifier.citationTugcu D., Gulec E. Y. , Akici F., Aydogan G., Salcioglu Z., Bayram C., Keskindemirci G., Bartsch O., "A Case of Rubinstein-Taybi Syndrome and Neuroblastoma with Heterozygous EX1 Deletion; Ex4-Ex16 Duplication Crebbp Mutation", PEDIATRIC BLOOD & CANCER, cilt.63, 2016
dc.identifier.issn1545-5009
dc.identifier.othervv_1032021
dc.identifier.otherav_b2d68f52-db63-461e-9a1c-9e9866a9787d
dc.identifier.urihttp://hdl.handle.net/20.500.12627/119108
dc.language.isoeng
dc.subjectİç Hastalıkları
dc.subjectHEMATOLOJİ
dc.subjectPEDİATRİ
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectOnkoloji
dc.subjectHematoloji
dc.subjectONKOLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.titleA Case of Rubinstein-Taybi Syndrome and Neuroblastoma with Heterozygous EX1 Deletion; Ex4-Ex16 Duplication Crebbp Mutation
dc.typeMakale
dc.relation.journalPEDIATRIC BLOOD & CANCER
dc.contributor.departmentIstanbul Kanuni Sultan Suleyman Training & Research Hospital , ,
dc.identifier.volume63
dc.contributor.firstauthorID236498


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