A microdeletion 22q11.2 can resemble Shprintzen–Goldberg omphalocele syndrome

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  • How to cite this article: Strenge S, Kujat A, Zelante L, Froster UG. 2006. A microdeletion 22q11.2 can resemble Shprintzen–Goldberg omphalocele syndrome. Am J Med Genet Part A 140A:2838–2839.

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Ancillary