The I1307KAPCPolymorphism: Prevalence in Non-Ashkenazi Jews and Evidence for a Founder Effect-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

The I1307KAPCPolymorphism: Prevalence in Non-Ashkenazi Jews and Evidence for a Founder Effect

Published:2001-06 Issue:2 Volume:5 Page:141-146
ISSN:1090-6576
Container-title:Genetic Testing
language:en
Short-container-title:Genetic Testing

Author:

Shtoyerman-Chen Rakefet¹,Friedman Eitan²,Figer Arie³,Carmel Miri¹,Patael Yael²,Rath Peter⁴,Fidder Herma H.¹,Bar-Meir Simon¹,Theodor Livia¹

Affiliation:

1. Department of Gastroenterology, Chaim Sheba Medical Center, Tel-Hashomer, Israel

2. The Susanne Levy Gertner Oncogenetics Unit, Chaim Sheba Medical Center, Tel-Hashomer, Israel

3. Institute of Oncology, Rabin Medical Center, Petah Tikvah, Israel

4. Institute of Oncology, Chaim Sheba Medical Center, Tel-Hashomer, Israel

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical)

Link

http://www.liebertpub.com/doi/pdf/10.1089/109065701753145628

Reference21 articles.

1. Could the 185delAG BRCA1 Mutation Be an Ancient Jewish Mutation?

2. The 185delAG BRCA1 mutation originated before the dispersion of Jews in the diaspora and is not limited to Ashkenazim

3. CA repeat polymorphism at the D5S82 locus, proximal to adenomatous polyposis coli (APC)

4. The Adenomatous Polyp and the Hereditary Polyposis Syndromes

5. Rapid diagnosis of beta-thalassemia mutations in Chinese by naturally and amplified created restriction sites

Cited by 27 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. Founder pathogenic variants in colorectal neoplasia susceptibility genes in Ashkenazi Jews undergoing colonoscopy;BJC Reports;2024-03-05

2. Position statement of the International Society for Gastrointestinal Hereditary Tumours (InSiGHT) onAPCI1307K and cancer risk;Journal of Medical Genetics;2023-04-19

3. Germline CDKN1B variant type and site are associated with phenotype in MEN4;Endocrine-Related Cancer;2023-01-01

4. Actionable genomic variants in 6045 participants from the Qatar Genome Program;Human Mutation;2021-09-02

5. Mutational analysis of candidate genes in Israeli male breast cancer cases;Breast Cancer Research and Treatment;2018-03-21

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