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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

Objective: We present molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a mentally retarded child of a family requesting for genetic counseling of the future pregnancy. Case report: A 43-year-old, gravida 1, para 1, woman, who had a 15-yea...

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Main Authors:	Chih-Ping Chen (Author), Schu-Rern Chern (Author), Peih-Shan Wu (Author), Shin-Wen Chen (Author), Fang-Tzu Wu (Author), Wayseen Wang (Author)
Format:	Book
Published:	Elsevier, 2021-03-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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