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Genetic associations of hemoglobin in children with chronic kidney disease in the PediGFR Consortium

dc.contributor.authorWarady, Bradley A.
dc.contributor.authorCaliskan, Salim
dc.contributor.authorKARABAY BAYAZIT, AYSUN
dc.contributor.authorSchaefer, Franz
dc.contributor.authorFurth, Susan L.
dc.contributor.authorAtkinson, Meredith A.
dc.contributor.authorXiao, Rui
dc.contributor.authorKoettgen, Anna
dc.contributor.authorWuehl, Elke
dc.contributor.authorWong, Craig S.
dc.contributor.authorWuttke, Matthias
dc.date.accessioned2021-03-05T08:19:05Z
dc.date.available2021-03-05T08:19:05Z
dc.date.issued2019
dc.identifier.citationAtkinson M. A. , Xiao R., Koettgen A., Wuehl E., Wong C. S. , Wuttke M., KARABAY BAYAZIT A., Caliskan S., Warady B. A. , Schaefer F., et al., "Genetic associations of hemoglobin in children with chronic kidney disease in the PediGFR Consortium", PEDIATRIC RESEARCH, cilt.85, ss.324-328, 2019
dc.identifier.issn0031-3998
dc.identifier.otherav_983ba68d-cfd9-41e4-a730-5c7be4b1407e
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/102450
dc.identifier.urihttps://doi.org/10.1038/s41390-018-0148-z
dc.description.abstractBACKGROUND: Genome-wide association studies (GWAS) in healthy populations have identified variants associated with erythrocyte traits, but genetic causes of hemoglobin variation in children with CKD are incompletely understood.
dc.language.isoeng
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleGenetic associations of hemoglobin in children with chronic kidney disease in the PediGFR Consortium
dc.typeMakale
dc.relation.journalPEDIATRIC RESEARCH
dc.contributor.departmentJohns Hopkins University , ,
dc.identifier.volume85
dc.identifier.issue3
dc.identifier.startpage324
dc.identifier.endpage328
dc.contributor.firstauthorID262310


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