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Diagnostic whole genome sequencing and split-read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndrome. (2014)

First Author: Watson CM

Attributed to: Infrastructure for collaboration: Leeds MRC Medical Bioinformatics Centre funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/ajmg.a.36679

PubMed Identifier: 25045150

Publication URI: http://europepmc.org/abstract/MED/25045150

Type: Journal Article/Review

Volume: 164A

Parent Publication: American journal of medical genetics. Part A

Issue: 10

ISSN: 1552-4825