Multiple Xbal polymorphisms for carrier detection and prenatal diagnosis of haemophilia A
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1989.tb00287.x/fullpdf
Reference11 articles.
1. Hemophilia A
2. Restriction fragment length polymorphisms associated with factor VIII: C gene in Chinese
3. Detection and sequence of mutations in the factor VIII gene of haemophiliacs
4. Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene
5. [49] DNA analysis in the diagnosis of hemoglobin disorders
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1. Hematological Practice in Hong Kong and China;Hematology/Oncology Clinics of North America;2016-04
2. Combined analysis of the MspI and XbaI polymorphisms in intron 22 of the factor VIII gene for detection of hemophilia A in a Korean population;Genetics and Molecular Research;2012
3. Hemophilia A: genetic prediction and linkage studies in all available families in Finland;Clinical Genetics;2008-06-28
4. Application of intron 9 and intron 25 dinucleotide repeats of the factor VIII gene for carrier diagnosis in haemophilia A;Haemophilia;2008-05
5. Analysis of the AluI polymorphism in intron 1 of the human coagulation factor VIII gene: A new marker for the hemophilia a carrier detection;Russian Journal of Genetics;2007-04
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