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