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SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia..
Am J Med Genet A
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Refining analyses of copy number variation identifies specific genes associated with developmental delay..
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Characterization of core clinical phenotypes associated with recurrent proximal 15q25.2 microdeletions..
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5q31.3 Microdeletion syndrome: clinical and molecular characterization of two further cases..
Am J Med Genet A
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