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dc.contributor.authorHershfield, Micheal
dc.contributor.authorKardas, Murat
dc.contributor.authorAygun, Deniz
dc.contributor.authorTORUN, EMEL
dc.contributor.authorCamcioglu, Yildiz
dc.contributor.authorTÜREL, Özden
dc.date.accessioned2021-03-05T07:56:54Z
dc.date.available2021-03-05T07:56:54Z
dc.date.issued2018
dc.identifier.citationTÜREL Ö., Aygun D., Kardas M., TORUN E., Hershfield M., Camcioglu Y., "A case of severe combined immunodeficiency caused by adenosine deaminase deficiency with a new mutation", PEDIATRICS AND NEONATOLOGY, cilt.59, ss.97-99, 2018
dc.identifier.issn1875-9572
dc.identifier.othervv_1032021
dc.identifier.otherav_9660a69d-f04e-4f2b-928b-bb5db55813f3
dc.identifier.urihttp://hdl.handle.net/20.500.12627/101220
dc.identifier.urihttps://doi.org/10.1016/j.pedneo.2016.10.008
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleA case of severe combined immunodeficiency caused by adenosine deaminase deficiency with a new mutation
dc.typeMakale
dc.relation.journalPEDIATRICS AND NEONATOLOGY
dc.contributor.departmentBezmiâlem Vakıf Üniversitesi , Tıp Fakültesi , Çocuk Sağlığı Ve Hastalıkları Anabilim Dalı
dc.identifier.volume59
dc.identifier.issue1
dc.identifier.startpage97
dc.identifier.endpage99
dc.contributor.firstauthorID251296


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