A HindIII RFLP and a gene lesion in the coagulation factor VIII gene-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

A HindIII RFLP and a gene lesion in the coagulation factor VIII gene

Published:1988-04 Issue:4 Volume:78 Page:359-362
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Bernardi F.,Legnani C.,Volinia S.,Patracchini P.,Rodorigo G.,DeRosa V.,Marchetti G.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00291736.pdf

Reference23 articles.

1. Antonarakis SE, Waber PG, Kittur SD, Patel AS, Kazazian HH, Mellis MA, Counts RB, Stamatoyannopoulos G, Bowie W, Fass DN, Pitmann DD, Wozney JM, Toole JJ (1985a) Hemophilia A. Detection of molecular defects and of carriers by DNA analysis. N Engl J Med 313:842?848

2. Antonarakis SE, Copeland KL, Carpenter RJ, Carta CA, Hoyer LW, Caskey CT, Toole JJ, Kazazian HH (1985b) Prenatal diagnosis of haemophilia A by factor VIII gene analysis. Lancet I:1407?1409

3. Bernardi F, Marchetti G, Bertagnolo V, Faggioli L, Volinia S, Patracchini P, Bartolai S, Vannini F, Felloni L, Rossi L, Panicucci F, Conconi F (1987) RFLP analysis in families with sporadic hemophilia A. Estimate of the mutation ratio in male and in female gametes. Hum Genet 76:253?256

4. Biggs R (1974) The absorption of human factor VIII neutralizing antibody by FVIII. Br J Haematol 26:259?267

5. Buffone GJ, Darlington GJ (1985) Isolation of DNA from biological specimens without extraction with phenol. Clin Chem 31:164?165

Cited by 17 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. A novel deletion of FVIII gene associated with variable levels of FVIII inhibitor*;European Journal of Haematology;2009-04-24

2. HindIII Polymorphism in Carrier Detection of Hemophilia A in India: A New Primer Design;Clinical and Applied Thrombosis/Hemostasis;2007-10

3. Rapid Polymerase Chain Reaction Analysis of St14 (DXS52) VNTR: Carrier Detection of Hemophilia A;Journal of Obstetrics and Gynaecology Research;1997-08

4. Polymorphisms associated with the FVIII and FIX genes in the Turkish population;Haemophilia;1995-07

5. Molecular etiology of factor VIII deficiency in hemophilia A;Human Mutation;1995

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3