Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1.

AUTOR(ES)

Barton, J S

RESUMO

We report an 18 month old girl with developmental delay, dysmorphic features, and a karyotype 46,XX,del (1) (p32.1p32.3). To our knowledge the clinical features associated with this deletion have not been reported previously.

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