A Familial Chromosomal Complex Rearrangement Confirms RUNX1T1 As a Causative Gene for Intellectual Disability and Suggests That 1p22.1p21.3 Duplication is Likely Benign.
Molecular Cytogenetics（2019）
关键词
Complex chromosomal rearrangements,RUNX1T1,1p22.1p21.3 duplication,8q21.3q22.1 deletion
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