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dc.contributor.authorDemirkol, M.
dc.contributor.authorMuntau, A.
dc.contributor.authorBelanger-Quintana, A.
dc.contributor.authorBlau, N.
dc.contributor.authorTrefz, F.
dc.contributor.authorFeillet, F.
dc.date.accessioned2022-02-18T10:57:45Z
dc.date.available2022-02-18T10:57:45Z
dc.identifier.citationTrefz F., Feillet F., Demirkol M., Muntau A., Belanger-Quintana A., Blau N., "SIGNIFICANCE OF NEONATAL BH4 LOADING FOR DIFFERENTIAL DIAGNOSIS OF HYPERPHENYLALANINEMIA", JOURNAL OF INHERITED METABOLIC DISEASE, cilt.35, 2012
dc.identifier.issn0141-8955
dc.identifier.othervv_1032021
dc.identifier.otherav_cb97e69c-453f-4582-8821-1a496b1a0e7f
dc.identifier.urihttp://hdl.handle.net/20.500.12627/180249
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTIP, ARAŞTIRMA VE DENEYSEL
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectResearch and Theory
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectEndocrinology, Diabetes and Metabolism
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectTıbbi Genetik
dc.subjectTıbbi Ekoloji ve Hidroklimatoloji
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectGenetics
dc.subjectEndocrinology
dc.subjectMolecular Biology
dc.subjectEndocrine and Autonomic Systems
dc.subjectReviews and References (medical)
dc.subjectGenetics (clinical)
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.titleSIGNIFICANCE OF NEONATAL BH4 LOADING FOR DIFFERENTIAL DIAGNOSIS OF HYPERPHENYLALANINEMIA
dc.typeMakale
dc.relation.journalJOURNAL OF INHERITED METABOLIC DISEASE
dc.contributor.departmentMVZ Kreisklin , ,
dc.identifier.volume35
dc.contributor.firstauthorID3380183


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