Pseudotrisomy 13 and autosomal recessive holoprosencephaly.

AUTOR(ES)

Seller, M J

RESUMO

Two sibs, diagnosed prenatally, had holoprosencephaly, midface hypoplasia, and normal chromosomes. The first fetus also had polydactyly. This sibship may represent an example of autosomal recessive pseudotrisomy 13.

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