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Whole genome sequencing for copy number variant detection... | ResearchHub
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Whole genome sequencing for copy number variant detection to improve diagnosis and management of rare diseases
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Authors
Pamela Bowman
6 more
Pamela Bowman
•
Hannah Grimes
4 more
•
Karen Low
Published
June 5, 2024
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Journal
Developmental Medicine & Child Neurology
Topics
Biology
Bioinformatics
Medicine
Pathology
Genomics
Show all topics
DOI
10.1111/dmcn.15985
License
CC-BY
Other Formats
PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Developmental Medicine & Child Neurology
Topics
Biology
Bioinformatics
Medicine
Pathology
Genomics
Show all topics
DOI
10.1111/dmcn.15985
License
CC-BY
Other Formats
PDF