A chromosome 1q22 microdeletion including ASH1L is associated with intellectual disability in a Chinese family

Overview of attention for article published in Molecular Cytogenetics, June 2020

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The proband discussed in this paper is of Chinese origin and inherited the ASH1L microdeletion from her father and exhibited the following phenotypes - #intellectualdisability #hypotonia #facialdysmorphism #dimentia #socialdysfunction #noonansyndrome http

A chromosome 1q22 microdeletion including ASH1L is associated with intellectual disability in a Chinese family. https://t.co/vRWLzRwaiC https://t.co/QwhKiB6iXD

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