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Case Reports
. 1989 Mar;32(3):420-4.
doi: 10.1002/ajmg.1320320331.

Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies

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Case Reports

Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies

C Turleau et al. Am J Med Genet. 1989 Mar.

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.

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