RFLP analysis in families with sporadic hemophilia A-Reference-Cited by-同舟云学术

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RFLP analysis in families with sporadic hemophilia A

Published:1987-07 Issue:3 Volume:76 Page:
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Bernardi F.,Marchetti G.,Bertagnolo V.,Faggioli L.,Volinia S.,Patracchini P.,Bartolai S.,Vannini F.,Felloni L.,Rossi L.,Panicucci F.,Conconi F.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00283618.pdf

Cited by 9 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. Human germline mutation in the factor IX gene;Mutation Research/DNA Repair;2001-11

2. Genetic, Biochemical, and Clinical Features of Chronic Granulomatous Disease;Medicine;2000-05

3. Genetic Analysis of 13 Families with X-Linked Chronic Granulomatous Disease Reveals a Low Proportion of Sporadic Patients and a High Proportion of Sporadic Carriers;Pediatric Research;1998-07

4. An Overview of Gene Alterations in Mild Hemophilia and Von Willebrand Disease;Desmopressin in Bleeding Disorders;1993

5. A recurrent missense mutation (Arg → Gln) and a partial deletion in factor VIII gene causing severe haemophilia A;British Journal of Haematology;1989-02

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