Browsing by Subject "Deletions"
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Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome
(Wellcome Open Research, 2020-08-04)Background: Large contiguous gene deletions at the distal end of the short arm of chromosome 9 result in the complex multi-organ condition chromosome 9p deletion syndrome. A range of clinical features can result from these ...