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Neuigkeiten Der Multimedia-Zeitschriftenlesesaal und der Kartenlesesaal in Leipzig sind vom 30.10. bis 03.11. geschlossen. // The multimedia/periodical reading room and the map reading room in Leipzig are closed from 30.10 to 03.11.
 
 
 


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Artikel 61 Human ferrochelatase: a novel mutation in patients with erythropoietic protoporphyria and an isoform caused by alternative splicing
Enthalten in Human genetics Bd. 95, Nr. 4, date:4.1995: 391-396
Online Ressource
Artikel 62 Molecular defects in erythropoietic protoporphyria with terminal liver failure
Enthalten in Human genetics Bd. 93, Nr. 6, date:6.1994: 711-713
Online Ressource
Artikel 63 IX. Aus den letzten Tagen der Kaiserin Elisabeth von Rußland
Enthalten in Historische Zeitschrift Bd. 36, 1876, Nr. 1: 419-432
Online Ressource
Artikel 64 A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Enthalten in Communications biology Bd. 5, 9.11.2022, Nr. 1, date:12.2022: 1-11
Online Ressource
Artikel 65 Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues
Enthalten in Acta neuropathologica Bd. 134, 6.7.2017, Nr. 6, date:12.2017: 889-904
Online Ressource
Artikel 66 Application of IVDr NMR spectroscopy to stratify Parkinson’s disease with absolute quantitation of blood serum metabolites and lipoproteins
Enthalten in Scientific reports Bd. 15, 22.5.2025, Nr. 1, date:12.2025: 1-20
Online Ressource
Artikel 67 A practical approach for the treatment of post-COVID symptoms
Enthalten in Herz Bd. 48, 23.4.2023, Nr. 3, date:6.2023: 243-246
Online Ressource
Artikel 68 Argatroban versus Lepirudin in critically ill patients (ALicia): a randomized controlled trial
Enthalten in Critical care Bd. 18, 25.10.2014, Nr. 5, date:10.2014: 1-8
Online Ressource
Artikel 69 Arterial tortuosity syndrome: 40 new families and literature review
Enthalten in Genetics in medicine Bd. 20, 11.1.2018, Nr. 10, date:10.2018: 1236-1245
Online Ressource
Artikel 70 Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings
Enthalten in Nature genetics Bd. 57, 24.6.2025, Nr. 7, date:7.2025: 1790-1791
Online Ressource


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