Deletion of the short arms of chromosome 20
- PMID: 965012
- DOI: 10.1007/BF00284443
Deletion of the short arms of chromosome 20
Abstract
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.