Hemophilia B: diagnostic value of RFLP analysis in 19 of the 20 known Finnish families-Reference-Cited by-同舟云学术

Hemophilia B: diagnostic value of RFLP analysis in 19 of the 20 known Finnish families

Published:2008-06-28 Issue:3 Volume:38 Page:187-197
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Lehesjoki Anna-Elina,Rasi Vesa,Chapelle Albert

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1990.tb03570.x/fullpdf

Reference39 articles.

1. Methods for the detection of haemophilia carriers: a memorandum;Akhmeteli;Bull. WHO,1977

2. The gene structure of human anti-hemophilic factor IX;Anson;EMBO J.,1984

3. Hemophilia A. Detection of molecular defects and of carriers by DNA analysis;Antonarakis;N. Engl. J. Med.,1985

4. Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families;Arveiler;Am. J. Hum. Genet.,1988

5. The molecular pathology of haemophilia B;Brownlee;Biochem. Soc. Trans.,1987

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1. Haemophilia B: From Molecular Diagnosis to Gene Therapy;Clinical Chemistry and Laboratory Medicine;2003-01-25

2. Carrier Testing of Children for Two X-Linked Diseases: A Retrospective Study of Comprehension of the Test Results and Social and Psychological Significance of the Testing;Pediatrics;2000-12-01

3. Carrier Testing of Children for Two X-Linked Diseases: A Retrospective Evaluation of Experience and Satisfaction of Subjects and Their Mothers;Genetic Testing;1999-01

4. HEMATOLOGIC DISORDERS IN PREGNANCY;Obstetrics and Gynecology Clinics of North America;1992-12