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Users may view, print, copy, and download text and data-mine the content in such documents, for the ...
Small gains and losses of chromosomal DNA, called copy number variants (CNVs), are the cause of many...
Genomic studies are increasingly revealing that neurodevelopmental disorders are caused by underlyin...
Contains fulltext : 136682.pdf (publisher's version ) (Closed access
A challenge in clinical genomics is to predict whether copy number variation (CNV) affecting a gene ...
Users may view, print, copy, download and text and data- mine the content in such documents, for the...
Purpose: Copy number variants have emerged as a major cause of human disease such as autism and inte...
Contains fulltext : 51726.pdf (publisher's version ) (Closed access
Genomic microarrays used to assess DNA copy number are now recommended as first-tier tests for the p...
Users may view, print, copy, and download text and data-mine the content in such documents, for the ...
Background: Array-comparative genomic hybridization (array-CGH) is a widely used technique to detect...
Despite improvements in sequencing technologies, DNA sequence variant interpretation for rare geneti...
Copy number variants (CNVs) are associated with many neurocognitive disorders; however, these events...
Changes in DNA copy number, whether confined to specific genes or affecting whole chromosomes, have ...
Microarray-based comparative genomic hybridization is a method of molecular analysis that identifies...
Users may view, print, copy, and download text and data-mine the content in such documents, for the ...
Small gains and losses of chromosomal DNA, called copy number variants (CNVs), are the cause of many...
Genomic studies are increasingly revealing that neurodevelopmental disorders are caused by underlyin...
Contains fulltext : 136682.pdf (publisher's version ) (Closed access
A challenge in clinical genomics is to predict whether copy number variation (CNV) affecting a gene ...
Users may view, print, copy, download and text and data- mine the content in such documents, for the...
Purpose: Copy number variants have emerged as a major cause of human disease such as autism and inte...
Contains fulltext : 51726.pdf (publisher's version ) (Closed access
Genomic microarrays used to assess DNA copy number are now recommended as first-tier tests for the p...
Users may view, print, copy, and download text and data-mine the content in such documents, for the ...
Background: Array-comparative genomic hybridization (array-CGH) is a widely used technique to detect...
Despite improvements in sequencing technologies, DNA sequence variant interpretation for rare geneti...
Copy number variants (CNVs) are associated with many neurocognitive disorders; however, these events...
Changes in DNA copy number, whether confined to specific genes or affecting whole chromosomes, have ...
Microarray-based comparative genomic hybridization is a method of molecular analysis that identifies...
Users may view, print, copy, and download text and data-mine the content in such documents, for the ...
Small gains and losses of chromosomal DNA, called copy number variants (CNVs), are the cause of many...
Genomic studies are increasingly revealing that neurodevelopmental disorders are caused by underlyin...