Restriction fragment length polymorphisms on the short arm of X chromosome among the Japanese population
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical)
Link
http://www.nature.com/articles/jhg198817.pdf
Reference19 articles.
1. Akita, Y., Ohno, S., Goto, J., Nakano, I., Takatsu, M., Sugita, H., and Suzuki, K. 1987. Diagnosis of Duchenne and Becker muscular dystrophies by DNA polymorphism.Jpn. J. Human Genet. 32:71–82.
2. Bakker, E., Hofker, M.H., Goor, N., Mandel, J.L., Wrogemann, K., Davies, K.E., Kunkel, L.M., Willard, H.F., Fenton, W.A., Sandkuyl, L., Majoor-Krakauer, D., Essen, A.J.v., Jahoda, M.G.J., Sachs, E.S., van Ommen, G.J.B., and Pearson, P.L. 1985. Prenatal diagnosis and carrier detection on Duchenne muscular dystrophy with closely linked RFLPs.Lancet 1: 655–658.
3. Blin, N. and Stafford, D.E. 1976. A general method for isolation of high molecular weight DNA from eukaryotes.Nucleic Acids Res. 3:2303–2308.
4. Burghes, A.H.M., Logan, C., Hu, X., Belfall, B., Worton, R.G., and Ray, P.N. 1987. A cDNA clone from the Duchenne/Becker muscular dystrophy gene.Nature 328:434–437.
5. Drayna, D. and White, R. 1985. The genetic linkage map of the human X chromosome.Science 230:753–758.
Cited by 5 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. 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
2. Carrier detection of duchenne/becker muscular dystrophy: Computer-assisted direct quantitation of gene amplification products;Brain and Development;1992-03
3. Population variation in molecular polymorphisms of the short arm of the human X chromosome;American Journal of Physical Anthropology;1991-07
4. Molecular-genetic study of Duchenne and Becker muscular dystrophies: Deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females;American Journal of Medical Genetics;1989-12
5. X Chromosome Restriction Fragment Length Polymorphisms in Five Racial Groups: Rare Variant Detected with the RC8 (DXS9) Probe in the Marathi Population, India;Human Heredity;1989
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