ICF Syndrome in Saudi Arabia: Immunological, Cytogenetic and Molecular Analysis-Reference-Cited by-同舟云学术

ICF Syndrome in Saudi Arabia: Immunological, Cytogenetic and Molecular Analysis

Published:2010-12-01 Issue:2 Volume:31 Page:245-252
ISSN:0271-9142
Container-title:Journal of Clinical Immunology
language:en
Short-container-title:J Clin Immunol

Author:

Kaya Namik,Al-Muhsen Saleh,Al-Saud Bandar,Al-Bakheet Albandary,Colak Dilek,Al-Ghonaium Abdulaziz,Al-Dhekri Hasan,Al-Mousa Hamoud,Arnaout Rand,Al-Owain Mohammad,Iqbal Mohammad

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Link

http://link.springer.com/content/pdf/10.1007/s10875-010-9488-0.pdf

Reference27 articles.

1. Brown DC, Grace E, Sumner AT, et al. ICF syndrome (immunodeficiency, centromeric instability and facial anomalies): investigation of heterochromatin abnormalities and review of clinical outcome. Hum Genet. 1995;96:411–6.

2. Jeanpierre M, Turleau C, Aurias A, et al. An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome. Hum Mol Genet. 1993;2:731–5.

3. Xu GL, Bestor TH, Bourc'his D, et al. Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene. Nature. 1999;402:187–91.

4. Wijmenga C, van den Heuvel LP, Strengman E, et al. Localization of the ICF syndrome to chromosome 20 by homozygosity mapping. Am J Hum Genet. 1998;63:803–9.

5. Wijmenga C, Hansen RS, Gimelli G, et al. Genetic variation in ICF syndrome: evidence for genetic heterogeneity. Hum Mutat. 2000;16:509–17.

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

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5. Vesicourethral reflux-induced renal failure in a patient with ICF syndrome due to a novelDNMT3Bmutation;American Journal of Medical Genetics Part A;2016-09-08