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You searched for: Author/Creator Annerén, G

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1. A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features. Issue 2 (17th December 2011)

9. The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q. Issue 5 (May 1997)