- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Hemophilia B: Genetic Variants and Carrier Detection ; volume:38 ; number:02 ; year:1977
Konferenz: VIth International Congress on Thrombosis and Haemostasis; 1977-06-27
Thrombosis and haemostasis ; 38, Heft 02 (1977)
- Contributor
-
Kasper, C.K.
Østerud, B.
Rapaport, S.I.
- DOI
-
10.1055/s-0039-1682645
- URN
-
urn:nbn:de:101:1-2019061209511817893109
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:00 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Kasper, C.K.
- Østerud, B.
- Rapaport, S.I.
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Genetic Variants of Hemophilia B.
Detection of Hemophilia a Carriers by Repeated Factor VIII Activity/Antigen Determinations
Preimplantation genetic diagnosis of hemophilia A
Pathogenic variants carrier screening in New Brunswick: Acadians reveal high carrier frequency for multiple genetic disorders
Gold nanoparticles for genetic therapy of hemophilia B
Insights into the Molecular Genetic of Hemophilia A and Hemophilia B: The Relevance of Genetic Testing in Routine Clinical Practice
Classifying Potential Carriers of Hemophilia: Report of the Joint WFH-WHO Expert Committee
Surgery in Hemophilia
Hemophilia in Norway
Molecular Diagnosis of Hemophilia A and Pathogenesis of Novel F8 Variants in Shanxi, China
Hemophilia carrier’s awareness, diagnosis, and management in emerging countries: a cross-sectional study in Côte d’Ivoire (Ivory Coast)
Carrier Detection in Hemophilia B.
Genetic Variants of Hemophilia B.
Detection of Hemophilia a Carriers by Repeated Factor VIII Activity/Antigen Determinations
Preimplantation genetic diagnosis of hemophilia A
Pathogenic variants carrier screening in New Brunswick: Acadians reveal high carrier frequency for multiple genetic disorders
Gold nanoparticles for genetic therapy of hemophilia B
Insights into the Molecular Genetic of Hemophilia A and Hemophilia B: The Relevance of Genetic Testing in Routine Clinical Practice
Classifying Potential Carriers of Hemophilia: Report of the Joint WFH-WHO Expert Committee
Surgery in Hemophilia
Hemophilia in Norway
Molecular Diagnosis of Hemophilia A and Pathogenesis of Novel F8 Variants in Shanxi, China