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...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Discover STM Publishing Ltd
2020-12-01
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| Series: | Journal of Biochemical and Clinical Genetics |
| Subjects: | |
| Online Access: | http://www.ejmanager.com/fulltextpdf.php?mno=116442 |