A case of de novo microdeletion with combination of 1q21.1 and 14q32.2q32.31

A case of de novo microdeletion with combination of 1q21.1 and 14q32.2q32.31

Background: Chromosomal microarray is considered as the first-line diagnostic genetic test in all individuals with intellectual disability (ID) and attention-deficit disorders. In recent years, the use of chromosomal microarrays routinely for this purpose has resulted in the identification of many n...

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Bibliographic Details
Main Authors:	Hale Onder Yilmaz, Kadri Karaer, Orkun Yilmaz
Format:	Article
Language:	English
Published:	Discover STM Publishing Ltd 2020-12-01
Series:	Journal of Biochemical and Clinical Genetics
Subjects:	1q21.1 microdeletion 14q32.2q32.31 microdeletion growth retardation
Online Access:	http://www.ejmanager.com/fulltextpdf.php?mno=116442

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