A new contribution to the study of 22 trisomy.

Humangenetik
A Pérez-CastilloV Aller

Abstract

The case of a 2 1/2-month-old male child with intrauterine distrophy features and multiple congenital malformations is presented. Cytogenetic studies of the child and his parents, completed with Q- and G-banding techniques led us to conclude that it is a case of 22 trisomy inherited from his mother.

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