SNX8 gene

A small 7p22.3 microdeletion: Case report of SNX8 haploinsufficiency and neurological findings 7p22.3 microdeletion, a small deletion within the short arm of chromosome 7, has been reported in the literature before, but the genotype-phenotype correlation remains uncertain. Clinical features in previous cases include developmental delay, intellectual disability, congenital heart disease,... Read More