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Detection of Clinically Relevant Copy Number Variations and Genes in a Bangladeshi Cohort of Neurodevelopmental Disorders

2021-10-01

Abstract excerpt

<h4>Background: </h4> Copy number variations (CNVs) play a critical role into the pathogenesis of neurodevelopmental disorders (NDD) among children. In this study, we aim to identify clinically relevant CNVs, genes and their phenotypic characteristics in an ethnically underrepresented homogenous population of Bangladesh. <h4>Methods: </h4>: We have conducted genome-wide chromosomal microarray analysis (CMA) for 21...

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Literature Corpus work
b7714248-50d7-572c-a355-6043551e063e
DOI
10.21203/rs.3.rs-948388/v1
Open publication

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