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Array-CGH in a boy with an occurrence of neurodevelopmental disorders and epilepsy

ABSTRACT: This analysis includes the whole-genome screening of unbalanced chromosomal rearrangements (copy-number variants; CNV) in a boy with neurodevelopmental disorders and epilepsy.

ORGANISM(S): Homo sapiens

SUBMITTER: Marketa Wayhelova

PROVIDER: E-MTAB-8147 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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