Spectrum of factor IX gene mutations causing haemophilia B from India

Author:

Ghosh Kanjaksha,Quadros Leera,Shetty Shrimati

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

Reference18 articles.

1. Molecular genotyping of the Italian cohort of patients with hemophilia B;Belvini;Haematologica,2005

2. A haemophilia A and B molecular genetic diagnostic programme in Hungary: a highly informative and cost-effective strategy;Klein;Haemophilia,2001

3. Haemophilia: strategies for carrier detection and prenatal diagnosis;Peake;Bull World Health Organ,1993

4. Identification of factor IX gene defects using a multiplex PCR and CSGE strategy: a first report;Jayandharan;J Thromb Haemost,2003

5. Molecular characterization of factor IX gene mutations in 53 patients with haemophilia B in India;Jayandharan;Thromb Haemost,2005

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