A strategy for carrier detection in Pakistani haemophilia B families

Author:

Imran M.1,Saeed M. T.2,Mahmood S.3,Mohsin S.2,Sohail S.4,Munir A.,Nazir H.

Affiliation:

1. Department of Physiology and Cell Biology; Centre for Research in Endocrinology and Reproductive Sciences (CRERS); University of Health Sciences (UHS)

2. Department of Hematology; UHS

3. Department of Human Genetics and Molecular Biology; UHS

4. Pakistan Haemophilia Welfare Association; Lahore; Pakistan

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Reference6 articles.

1. Haemophilias A and B;Bolton-Maggs;Lancet,2003

2. Haemophilia A and haemophilia B: Molecular insights;Bowen;J Clin Pathol: Mol Pathol,2002

3. Haemophilia: Strategies for carrier detection and prenatal diagnosis;Peake;Bull WHO,1993

4. First-trimester prenatal diagnosis in haemophilia A and B families: 10 years experience from a centre in India;Shetty;Prenat Diagn,2006

5. Screening of intron 1 inversion and three intragenic factor VIII gene polymorphisms in Pakistani hemophilia A families;Bugvi;Blood Coagul Fibrin,2012

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Diagnosis and phenotypic assessment of Pakistani Haemophilia B carriers;Pakistan Journal of Medical Sciences;2017-06-02

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