Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autism and congenital heart defects

Chen, CP; Chern, SR; Wu, PS; Chen, SW; Wu, FT; Wang, W

Chen, CP (corresponding author), MacKay Mem Hosp, Dept Obstet & Gynecol, 92,Sect 2,Chung Shan North Rd, Taipei 104215, Taiwan.

TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2021; 60 (2): 341

Abstract

Objective: We present molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a mentally retard......

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