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Published in 2020 at "Frontiers in Genetics"
DOI: 10.3389/fgene.2020.00561
Abstract: In this report, we present a patient with brain alterations and dysmorphic features associated with chromosome duplication seen in 4p16.3 region and chromosomal deletion in a critical region responsible for Cri-du-chat syndrome (CdCS). Chromosomal microarray…
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Keywords:
neurological findings;
associated neurological;
patient trisomy;
candidate genes ... See more keywords