Carrier analysis for hemophilia A: ideal versus acceptable
Author:
Publisher
Informa UK Limited
Subject
Genetics,Molecular Biology,Molecular Medicine,Pathology and Forensic Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1586/erm.09.3
Reference33 articles.
1. Haemophilias A and B
2. Screening for Hemophilia A Carriers: Utility of PCR-RFLP—Based Polymorphism Analysis
3. An Improved Method for Prenatal Diagnosis of Genetic Diseases by Analysis of Amplified DNA Sequences
4. The utility of a HindIII polymorphism of factor VIII examined by rapid DNA analysis
5. Mutations and a polymorphism in the factor VIII gene discovered by denaturing gradient gel electrophoresis.
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1. Association of Genetic Variant FVIII Gene and Factor VIII: A Pilot Study Among Hemophilia A Female Relatives in Saudi Arabia;Cureus;2023-07-17
2. HindIII and MseI in the Biomolecular Profile of Hemophilia in Cameroon: A Primer Study;Journal of Biosciences and Medicines;2022
3. Determining common variants in patients with haemophilia A in South Vietnam and screening female carriers in their family members;Journal of Clinical Pathology;2021-11-29
4. Haemophilia: A disease of women as well;South African Journal of Child Health;2016-03-29
5. Carrier and prenatal diagnostic strategy and newly identified mutations in Hungarian haemophilia A and B families;Blood Coagulation & Fibrinolysis;2015-03
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