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Living with a child at risk for psychotic illness: The experience of parents coping with 22q11 deletion syndrome: An exploratory study. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Aug 12.
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A 10.7 Mb interstitial deletion of 13q21 without phenotypic effect defines a further non-pathogenic euchromatic variant. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Aug 12.
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Analysis of the Prader-Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) array. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Aug 12.
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