Day

February 6, 2020

06
Feb

A small 7p22.3 microdeletion: Case report of SNX8 haploinsufficiency and neurological findings

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,...
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