A 5q12.1–5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

A 5q12.1–5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement

Published:2013-03 Issue:1 Volume:516 Page:176-180
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Cetin Zafer,Yakut Sezin,Clark Ozden Altiok,Mihci Ercan,Berker Sibel,Luleci Guven

Funder

Akdeniz University Scientific Projects Management Unit

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference18 articles.

1. Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort;Baptista;Am. J. Hum. Genet.,2008

2. A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation;Borg;J. Med. Genet.,2002

3. Interstitial deletion of 13q22–q32: a case with choanal atresia and mega-cisterna magna and review of the literature;Cetin;Genet. Couns.,2011

4. A constitutional complex chromosome rearrangement involving meiotic arrest in an azoospermic male: case report;Coco;Hum. Reprod.,2004

5. Identification of a 650 kb duplication at the X chromosome breakpoint in a patient with 46, X, t(X;8)(q28;q12) and non-syndromic mental retardation;Cox;J. Med. Genet.,2003

Cited by 9 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. Genome-wide association study identifies quantitative trait loci affecting cattle temperament;Zoological Research;2022

2. Cytogenetic and Array-CGH Characterization of a Simple Case of Reciprocal t(3;10) Translocation Reveals a Hidden Deletion at 5q12;Genes;2021-06-07

3.

Identification of High-Frequency Methylation Sites in RNF180 Promoter Region Affecting Expression and Their Relationship with Prognosis of Gastric Cancer

;Cancer Management and Research;2020-05

4. The influence of balanced complex chromosomal rearrangements on preimplantation embryonic development potential and molecular karyotype;BMC Genomics;2020-04-29

5. Familial 5q12.3 Microdeletion: Evidence for a Locus Associated with Epilepsy;Molecular Syndromology;2017

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