Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG Island, and no clear phenotypic association-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG Island, and no clear phenotypic association

Published:1992-04-15 Issue:1-2 Volume:43 Page:224-231
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Oberlé I.,Boué J.,Croquette M. F.,Voelckel M. A.,Mattei M. G.,Mandel J. L.

Publisher

Wiley

Subject

Genetics(clinical)

Reference15 articles.

1. FRAGILE X IN A NORMAL MALE: A CAUTIONARY TALE

2. (1992) Two families with Xq27.3 fragility, no detectable insert in the FMR-1 gene, mild mental impairment and absence of the Martin-Bell phenotype. Am J Med Genet, this issue.

3. Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n

4. Association of the Robin sequence with the fragile X syndrome

5. Molecular heterogeneity of the fragile X syndrome

Cited by 14 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. Fragile X-Linked Mental Retardation;Encyclopedia of Molecular Cell Biology and Molecular Medicine;2006-09-15

2. Rare fragile sites;Cytogenetic and Genome Research;2003

3. Immunocytochemical and Biochemical Characterization of FMRP, FXR1P, and FXR2P in the Mouse;Experimental Cell Research;2000-07

4. Screening for Fragile X Syndrome: Information Needs for Health Planners;Journal of Medical Screening;1997-06

5. Unstable triplet repeat sequences: A source of cancer mutations?;STEM CELLS;1995-01

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