Screening of deletions and RFLP analysis in Turkish DMD/BMD families by PCR
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1993.tb03814.x/fullpdf
Reference26 articles.
1. A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridization shows mistypinas by both methods;Abbs;J Med Genet,1991
2. Detection of 98% of DMD/BMD deletions by PCR;Beggs;Hum Genet,1990a
3. A polymorphic CACA repeat in the 3′untranslated region of dystrophin;Beggs;Nucleic Acids Res,1990b
4. 242 breakpoints in the 200-kb deletion prone F20 region of the DMD gene are widely spread;Blonden;Genomics,1991
5. Point mutation in the human dystrophin gene; identification through Western blot analysis;Bulman;Genomics,1991a
Cited by 7 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. Identification of the parental origin of polysomy in two 49,XXXXY cases;Clinical Genetics;2008-06-28
2. Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patients;Pediatrics International;2008-04
3. Molecular characterisation of Duchenne muscular dystrophy and phenotypic correlation;Journal of the Neurological Sciences;1998-05
4. Distribution of dystrophin gene deletions mapped by multiplex PCR in the Moravian population;Molecular and Cellular Probes;1997-02
5. Allele frequencies of intragenic, and 5′ and 3′ markers of the dystrophin gene in Japanese families afflicted with Duchenne or Becker muscular dystrophy;Japanese Journal of Human Genetics;1996-12
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