The use of DNA markers for carrier detection and prenatal diagnosis of haemophilia A in Egyptian families-Reference-Cited by-同舟云学术

The use of DNA markers for carrier detection and prenatal diagnosis of haemophilia A in Egyptian families

Published:2008-09 Issue:5 Volume:14 Page:1082-1087
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:

Author:

HUSSEIN I. R.,EL-BESHLAWY A.,SALEM A.,MOSAAD R.,ZAGHLOUL N.,RAGAB L.,FAYEK H.,GABER K.,EL-EKIABI M.

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2008.01779.x/fullpdf

Reference29 articles.

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2. Genetic diagnosis of haemophilia and other inherited bleeding disorders;Peyvandi;Haemophilia,2006

3. Carrier detection in non deletional Duchenne/ Becher muscular dystrophy families using polymorphic dinucleotide (CA) repeat loci of dystrophin gene;Chaturvedi;Indian J Med Res,2001

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