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- W2415344127 abstract "Patients presenting with infantile spasms, dysmorphic features, and periventricular nodular heterotopia may benefit from genetic copy number variation microarray, or whole-exome sequencing to identify candidate genes. This will allow personalized diagnosis and prognostication and the eventual understanding of single and combined gene functions in brain health and disease." @default.
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- W2415344127 date "2016-06-03" @default.
- W2415344127 modified "2023-10-07" @default.
- W2415344127 title "Infantile spasms with periventricular nodular heterotopia, unbalanced chromosomal translocation 3p26.2 ‐10p15.1 and 6q22.31 duplication" @default.
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- W2415344127 doi "https://doi.org/10.1002/ccr3.591" @default.
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