https://elifesciences.org/articles/58178/figures
A model of in vitro human corticogenesis identifies alterations in gene expression caused by loss of 16p11.2 CNV genes in hiPSC-derived progenitor cells.
figuresdatamicrodeletiontranscriptionalalterations
https://pubmed.ncbi.nlm.nih.gov/30615951/
Xia-Gibbs syndrome is a rare genetic condition characterized by intellectual disability, growth retardation, delayed psychomotor development with absent or...
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