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Title: Pseudotrisomy 13 and autosomal recessive holoprosencephaly. Author: Seller MJ, Chitty LS, Dunbar H. Journal: J Med Genet; 1993 Nov; 30(11):970-1. PubMed ID: 8301659. Abstract: 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.[Abstract] [Full Text] [Related] [New Search]