Delineation of supernumerary marker chromosomes in 38 patients
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference40 articles.
1. Marker chromosomes in parents to children with Down's syndrome
2. 48,XY,21+, mar+mat: a case of trisomy 21 associated with an inherited small marker chromosome.
3. Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescencein situ hybridization
4. Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization
5. Forty four probands with an additional ?marker? chromosome
Cited by 55 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. Hypogonadotropic hypogonadism associated with another small supernumerary marker chromosome (sSMC) derived from chromosome 22, a case report;Translational Andrology and Urology;2021-04
2. Analysis of molecular cytogenetic features and PGT-SR for two infertile patients with small supernumerary marker chromosomes;Journal of Assisted Reproduction and Genetics;2019-11-12
3. Complex Small Supernumerary Marker Chromosome Leading to Partial 4q/21q Duplications: Clinical Implication and Review of the Literature;Cytogenetic and Genome Research;2018
4. Impaired Spermatogenesis due to Small Supernumerary Marker Chromosomes: The Reason for Infertility Is Only Reliably Ascertainable by Cytogenetics;Sexual Development;2018
5. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21;Taiwanese Journal of Obstetrics and Gynecology;2017-08
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