Direct carrier detection in hemophilia B kindreds: Use of modified primers (mutagenic primers) for enzymatic amplification of the factor IX gene-Reference-Cited by-同舟云学术

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Direct carrier detection in hemophilia B kindreds: Use of modified primers (mutagenic primers) for enzymatic amplification of the factor IX gene

Published:1991-08 Issue:3 Volume:63 Page:355-361
ISSN:0049-3848
Container-title:Thrombosis Research
language:en
Short-container-title:Thrombosis Research

Author:

Matsushita Tadashi,Tanimoto Mitsune,Yamamoto Koji,Sugiura Isamu,Takamatsu Junki,Kamiya Tadashi,Saito Hidehiko

Publisher

Elsevier BV

Subject

Hematology

Reference24 articles.

1. Characterization and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (Factor IX deficiency);Gianneli;Lancet,1984

2. Use of Bam HI polymorphism in the factor IX gene for the determination of hemophilia B carrier status;Hay;Blood,1986

3. The use of DNA amplification for genetic counselling related diagnosis in hemophilia B;Tsang;Thromb Haemost,1989

4. Detection of polymorphisms at cytosine phosphoguanidine dinucleotides and diagnosis of hemophilia B carriers;Winship;Lancet,1989

5. Possible absence of common polymorphisms in coagulation factor IX gene in Japanese subjects;Kojima;Blood,1987

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic Predisposition to β-Thalassemia and Sickle Cell Anemia in Turkey: A Molecular Diagnostic Approach;Methods in Molecular Biology;2010-11-07

2. Haematology;Clinical Science;1994-08-01

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