A novel 800 kb microduplication of chromosome 16q22.1 resulting in learning disability and epilepsy may explain phenotypic variability in a family with 15q13 microdeletion

Siddharth Banka, Gregory J. Fitzgibbon, Lorraine Gaunt, Wendy J. Rankin, Jill Clayton-Smith

Research output: Contribution to journal › Article › peer-review

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Biochemistry, Genetics and Molecular Biology

Neuroscience