Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers

Author:

Kwan Sau-Ping,Sandkuyl Lodewijk A.,Blaese Michael,Kunkel Louis M.,Bruns Gail,Parmley Robin,Skarshaug Shannon,Page David C.,Ott Jurg,Rosen Fred S.

Publisher

Elsevier BV

Subject

Genetics

Reference26 articles.

1. A strategy to reveal high-frequency RFLPs along the human X chromosome;Aldridge;Amer. J. Hum. Genet,1984

2. Genetic mapping of nine DNA markers in the q11–q22 region of the human X chromosome;Arveiller;Genomics,1987

3. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs;Bakker;Lancet,1985

4. A mileage chart of part of the X chromosome;Bhattacharya,1988

5. Isolation of X chromosomes DNA sequences;Bruns;Adv. Exp. Med. Biol,1982

Cited by 48 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. Gene Therapy for Inborn Errors of Immunity;The Journal of Allergy and Clinical Immunology: In Practice;2023-06

2. Wiskott Aldrich Syndrome: Short Review;Sağlık Bilimlerinde Değer;2023-05-10

3. Discovering the Cause of Wiskott–Aldrich Syndrome and Laying the Foundation for Understanding Immune Cell Structuring;The Journal of Immunology;2018-05-21

4. Clinical Manifestations and Pathophysiological Mechanisms of the Wiskott-Aldrich Syndrome;Journal of Clinical Immunology;2017-10-30

5. MICROTHROMBOCYTOPENIA IN A MALE INFANT WITH CYTOMEGALOVIRUS;Annals of Allergy, Asthma & Immunology;2009-09

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