A FISH study of chromosome fusion in the ICF syndrome: involvement of paracentric heterochromatin but not of the centromeres themselves.

Author:

Sumner A T,Mitchell A R,Ellis P M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference10 articles.

1. ICF syndrome: a new case and review of the literature;Smeets, D.F.C.M.; Moog, U.; Weemaes, C.M.R.;Hum Genet,1994

2. ICF syndrome (immunodeficiency, centromeric instability and facial anomalies): investigation of heterochromatin abnormalities and review of clinical outcome;Brown, D.C.; Grace, E.; Sumner, A.T.; Edmunds, A.T.; Ellis, P.M.;Hum Genet,1995

3. FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor;true;Hum Genet,1995

4. ICF syndrome with variable expression in sibs;Gimelli, G.; Varone, P.; Pezzolo, A.; Lerone, M.; Pistoia, V.;J Med Genet,1993

5. Chromosome banding;Sumner, A.T.,1990

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