DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor-Reference-Cited by-同舟云学术

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DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor

Published:1995-11 Issue:5 Volume:96 Page:562-571
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Schuffenhauer Simone,Bartsch Oliver,Stumm Markus,Buchholz Tina,Petropoulou Theoni,Kraft Sabine,Belohradsky Bernd,Klaus Hinkel Georg,Meitinger Thomas,Wegner Rolf-Dieter

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00197412.pdf

Cited by 53 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. Screening Newborns for Low T Cell Receptor Excision Circles (TRECs) Fails to Detect Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome;The Journal of Allergy and Clinical Immunology: In Practice;2023-09

2. Epigenetic syndromes with immune deficiency;Stiehm's Immune Deficiencies;2020

3. DNA methylation in disease: Immunodeficiency, Centromeric instability, Facial anomalies syndrome;Essays in Biochemistry;2019-11-14

4. The gene mutations and subtelomeric DNA methylation in immunodeficiency, centromeric instability and facial anomalies syndrome;Autoimmunity;2019-08-18

5. Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey;Journal of Clinical Immunology;2016-02

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