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  1. Article

    Open Access

    Constitutional 763.3 Kb chromosome 1q43 duplication encompassing only CHRM3 gene identified by next generation sequencing (NGS) in a child with intellectual disability

    Deletion or duplication on the distal portion of the long arm of chromosome 1 result in complex and highly variable clinical phenotype including.

    **aofei Cheng, Qifang Yang, Jun Liu, Juan Ye, Huiying **ao… in Molecular Cytogenetics (2019)

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