Characterization of mosaic supernumerary ring chromosomes by array-CGH: Segmental aneusomy for proximal 4q in a child with tall stature and obesity-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Characterization of mosaic supernumerary ring chromosomes by array-CGH: Segmental aneusomy for proximal 4q in a child with tall stature and obesity

Published:2006-02-01 Issue:3 Volume:140A Page:233-237
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Bonnet Céline,Zix Christian,Grégoire Marie-José,Brochet Karène,Duc Mireille,Rousselet Florence,Philippe Christophe,Jonveaux Philippe

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference20 articles.

1. Insulin-like growth factor axis during embryonic development

2. Multiple supernumerary ring chromosomes of different origin in a patient: A clinical report and review of the literature

3. Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization

4. Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes

5. A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man.

Cited by 16 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. Syndromic obesity with neurodevelopmental delay: Opportunities for targeted interventions;European Journal of Medical Genetics;2022-03

2. A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature;Genes;2021-12-07

3. Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report;International Journal of Reproductive BioMedicine (IJRM);2021-06-23

4. Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1–q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality;Taiwanese Journal of Obstetrics and Gynecology;2017-04

5. Interstitial microdeletions including the chromosome band 4q13.2 and theUBA6gene as possible causes of intellectual disability and behavior disorder;American Journal of Medical Genetics Part A;2015-08-18

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

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