Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene-Reference-Cited by-同舟云学术

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

Published:1999-11 Issue:6758 Volume:402 Page:187-191
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Xu Guo-Liang,Bestor Timothy H.,Bourc'his Déborah,Hsieh Chih-Lin,Tommerup Niels,Bugge Merete,Hulten Maj,Qu Xiaoyan,Russo James J.,Viegas-Péquignot Evani

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/46052.pdf

Reference29 articles.

1. Maraschio,P., Zuffardi,O., Dalla Fior,T. & Tieplo,L. Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies; the ICF syndrome. J. Med. Genet. 25, 173–180 (1988).

2. Hulten,M. Selective somatic pairing and fragility at 1q12 in a boy with common variable immunodeficiency. Clin. Genet. 14, 294 (1978).

3. Tieplo,L. et al. Concurrent instability at specific sites of chromosomes 1, 9, and 16 resulting in multibranched chromosomes. Clin. Genet. 14, 313–314 (1978).

4. Jeanpierre,M. et al. An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome. Hum. Mol. Genet. 2, 731–735 (1993).

5. Okano,M., Xie,S. & Li,E. Cloning and characterization of a family of novel mammalian DNA (cytosine-5)-methyltransferases. Nature Genet. 19, 219–220 (1998).

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