Multibranched chromosomes in the ICF syndrome: Immunodeficiency, centromeric instability, and facial anomalies
- 1 March 1989
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 32 (3) , 420-424
- https://doi.org/10.1002/ajmg.1320320331
Abstract
A new patient with the rare ICF syndrome (immunodeficiency, centromeric heterochromatin instability, and facial anomalies) is reported. The six patients previously reported in the literature are reviewed. The main clinical and cytogenetic characteristics of the syndrome are discussed.Keywords
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