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Deletion of the short arms of chromosome 20
Authors:Dagmar K Kalousek  Serge Thérien
Institution:(1) Douglas Cytogenetic Laboratory, Department of Pathology, Montreal Children's Hospital, Montreal, Canada;(2) Department of Medical Genetics, Montreal Children's Hospital, Montreal, Canada
Abstract:Summary A 46, XX, del(20) (p11) karyotype (Paris Conference, 1971) was identified in an 11-month-old French-Canadian girl with a dysmorphic syndrome, multiple congenital anomalies, psychomotor and growth retardation. Both parents had normal phenotype and karyotype.
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