Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2006.01431.x/fullpdf
Reference33 articles.
1. Mutation Analysis in F9 Gene of 17 Families with Haemophilia B from Iran
2. DNA microarray analysis for the detection of mutations in hemophilia A
3. Factor VIII and IX gene polymorphisms and carrier analysis in Indian population
4. Prenatal diagnosis in hemophilia A using factor VIII gene polymorphism?Indian experience
5. Informativeness of linkage analysis for genetic diagnosis of haemophilia A in India
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1. Prenatal diagnosis in rare bleeding disorders-An unresolved issue?;International Journal of Laboratory Hematology;2018-02-24
2. Factor VII Deficiency: Clinical Phenotype, Genotype and Therapy;Journal of Clinical Medicine;2017-03-28
3. The activity of factor VIII and IX of cord blood at mid-trimester in fetuses without hemophilia;Journal of Genetic Medicine;2016-12-31
4. Factor VII Deficiency: From Basics to Clinical Laboratory Diagnosis and Patient Management;Clinical and Applied Thrombosis/Hemostasis;2016-10-03
5. Second trimester prenatal diagnosis in Glanzmann's Thrombasthenia;Haemophilia;2015-12-28
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