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Additional file 1 of Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases (2024)

First Author: Pagnamenta A

Attributed to: Switching mammalian genes on and off during development, lineage specification, and differentiation, and its impact on human genetic disease funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.6084/m9.figshare.26990311.v1

Publication URI: https://springernature.figshare.com/articles/journal_contribution/Additional_file_1_of_Structural_and_non-coding_variants_increase_the_diagnostic_yield_of_clinical_whole_genome_sequencing_for_rare_diseases/26990311/1

Type: Other