Carrier detection and prenatal diagnosis in haemophilia in India: realities and challenges-Reference-Cited by-同舟云学术

Carrier detection and prenatal diagnosis in haemophilia in India: realities and challenges

Published:2002-01 Issue:1 Volume:8 Page:51-55
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:

Author:

GHOSH K.,SHETTY S.,PAWAR A.,MOHANTY D.

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2516.2002.00576.x/fullpdf

Reference22 articles.

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2. Haemophilia A database of nucleotide substitutions, deletions, insertions and reaarangements of the factor VIII gene;Tuddenham;Nucl Acids Res,1994

3. Carrier detection in haemophilia A families. Comparison of conventional coagulation parameter with DNA polymorphism analysis results - first report from India;Shetty;Haemophilia,1999

4. Determination of the von Willebrand's disease antigen (factor VIII related antigen) in plasma by quantitative immunoelectrophoresis;Zimmerman;J Lab Clin Med,1975

5. Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A;Lakich;Nat Gen,1993

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