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Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies
C Turleau1, M O Cabanis, D Girault
1U.173 INSERM-Cytogénétique Humaine et Comparée, Hôpital Necker-Enfants-Malades, Paris, France.
American Journal of Medical Genetics
|March 1, 1989
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.