- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Genetic Variants of Hemophilia B. ; 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
-
Roberts, H.R.
Chung, K.S.
Goldsmith, J.C.
- DOI
-
10.1055/s-0039-1682644
- URN
-
urn:nbn:de:101:1-2019061209305135859496
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:59 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
- Roberts, H.R.
- Chung, K.S.
- Goldsmith, J.C.
Other Objects (12)
Hemophilia B: Genetic Variants and Carrier Detection
Preimplantation genetic diagnosis of hemophilia A
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
Molecular Diagnosis of Hemophilia A and Pathogenesis of Novel F8 Variants in Shanxi, China
Measuring hemophilia caregiver burden: validation of the Hemophilia Caregiver Impact measure
Investigations on genetic variants of fibrinogen
Analysis of rare genetic variants in genetic generalized epilepsies
Hemophilia in Norway
Surgery in Hemophilia
Perioperative Management of Hemophilia Patients
Dystrophin genetic variants and autism
Hemophilia B: Genetic Variants and Carrier Detection
Preimplantation genetic diagnosis of hemophilia A
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
Molecular Diagnosis of Hemophilia A and Pathogenesis of Novel F8 Variants in Shanxi, China
Measuring hemophilia caregiver burden: validation of the Hemophilia Caregiver Impact measure
Investigations on genetic variants of fibrinogen
Analysis of rare genetic variants in genetic generalized epilepsies
Hemophilia in Norway
Surgery in Hemophilia
Perioperative Management of Hemophilia Patients
Dystrophin genetic variants and autism
Hemophilia B: Genetic Variants and Carrier Detection
Preimplantation genetic diagnosis of hemophilia A
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
Molecular Diagnosis of Hemophilia A and Pathogenesis of Novel F8 Variants in Shanxi, China
Measuring hemophilia caregiver burden: validation of the Hemophilia Caregiver Impact measure
Investigations on genetic variants of fibrinogen
Analysis of rare genetic variants in genetic generalized epilepsies
Hemophilia in Norway
Surgery in Hemophilia
Perioperative Management of Hemophilia Patients