The following article for this Special Issue was previously published and can be found in their respective issues or online. Issue 9 (25th January 2020)

Record Type:: Journal Article
Title:: The following article for this Special Issue was previously published and can be found in their respective issues or online. Issue 9 (25th January 2020)
Main Title:: The following article for this Special Issue was previously published and can be found in their respective issues or online
Editors:: Moult, John
Brenner, Steven E.
Other Names:: Karchin Rachel guestEditor.
Pal Lipika R. specialEditor.
Abstract:: Abstract : Matching whole genomes to rare genetic disorders: Identification of potential causative variants using phenotype‐weighted knowledge in the CAGI SickKids5 clinical genomes challenge (41: 2) https://onlinelibrary.wiley.com/doi/10.1002/humu.23933
Is Part Of:: Human mutation. Volume 40:Issue 9(2019)
Journal:: Human mutation
Issue:: Volume 40:Issue 9(2019)
Issue Display:: Volume 40, Issue 9 (2019)
Year:: 2019
Volume:: 40
Issue:: 9
Issue Sort Value:: 2019-0040-0009-0000
Page Start:: N/A
Page End:: N/A
Publication Date:: 2020-01-25
Subjects:: Human chromosome abnormalities -- Periodicals
Mutation (Biology) -- Periodicals
616.04205
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-1004 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/humu.23090 ↗
Languages:: English
ISSNs:: 1059-7794
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 4336.217000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 12682.xml