Terminal deletion of the long arm of chromosome 10.

AUTOR(ES)

Curtis, H

RESUMO

A de novo chromosome abnormality interpreted as a terminal deletion of chromosome 10, del(10)(pter----q25.2:), was ascertained in a newborn female with multiple malformations. The clinical features observed at birth and on follow up at 10 months of age are described and compared with previously reported cases.

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