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A Complex Neurodevelopmental Phenotype Resembling a Chromatinopathy With Concurrent 7p Duplication and 10p Deletion Involving ZMYND11: A Case Report and Literature Review.

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Title: A Complex Neurodevelopmental Phenotype Resembling a Chromatinopathy With Concurrent 7p Duplication and 10p Deletion Involving ZMYND11: A Case Report and Literature Review.
Authors: Minale, Elia Marco Paolo1 (AUTHOR), Martone, Stefania2 (AUTHOR), Criscuolo, Chiara3,4 (AUTHOR), Marra, Roberta5,6 (AUTHOR), Lasorsa, Vito Alessandro5,6 (AUTHOR), Ruggiero, Raffaella7 (AUTHOR), Suero, Teresa7 (AUTHOR), Capasso, Mario5,6 (AUTHOR), Andolfo, Immacolata5,6 (AUTHOR), Iolascon, Achille5,6 (AUTHOR), Russo, Roberta5,6 (AUTHOR), Pinelli, Michele2,5,6 (AUTHOR) michele.pinelli@unina.it
Source: Molecular Genetics & Genomic Medicine. Apr2026, Vol. 14 Issue 4, p1-6. 6p.
Database: Academic Search Ultimate
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              Text: Apr2026
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