Chromosomal Translocation in a Mentally Deficient Child with Cryptorchidism
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1963.tb03762.x/fullpdf
Reference15 articles.
1. Chromosome Anomaly in Two Cases of Cerebral Palsy, a Brother and a Sister
2. Association Between Congenital Heart Malformation and Chromosomal Variations
3. CHROMOSOME TRANSLOCATION AS A CAUSE OF FAMILIAL MONGOLISM
4. CHROMOSOMAL ABNORMALITIES IN FATHER AND MONGOL CHILD
5. The chromosomal etiology of congenital gonadal defects
Cited by 33 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. DERMATOGLYPHICS IN PRADER-WILLI SYNDROME;Journal of Intellectual Disability Research;2008-06-28
2. PRADER-WILLI SYNDROME;Journal of Intellectual Disability Research;2008-06-28
3. Prader-Willi Syndrome with del(15)(q1l, q13) Associated with Hepatoblastoma;Pediatrics International;1991-12
4. Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome;American Journal of Medical Genetics;1986-03
5. Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment;Human Genetics;1983-10
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