Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder
Article in Molecular Cytogenetics (June 2020)
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High-purity isolation of rare single cells from blood using a tiered microchip system
Article in PLOS ONE (March 2020)
Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature
Article in Molecular Cytogenetics (February 2018)