Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2

N H Robin G J Feldman; A L Aronson; H F Mitchell; R Weksberg; C O Leonard; B K Burton; K D Josephson; R Laxova; K A Aleck; J E Allanson

New York v.11, n.4, p.459-61, 1995 Nature Genetics

New York 1995

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