Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X‐linked microcephalic intellectual deficit. (19th April 2013)

Record Type:: Journal Article
Title:: Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X‐linked microcephalic intellectual deficit. (19th April 2013)
Main Title:: Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X‐linked microcephalic intellectual deficit
Authors:: Ariani, F
Mari, F
Amitrano, S
Di Marco, C
Artuso, R
Scala, E
Meloni, I
Della Volpe, R
Rossi, A
van Bokhoven, H
Renieri, A
Abstract:
Is Part Of:: Clinical genetics. Volume 83:Number 3(2013:Mar.)
Journal:: Clinical genetics
Issue:: Volume 83:Number 3(2013:Mar.)
Issue Display:: Volume 83, Issue 3 (2013)
Year:: 2013
Volume:: 83
Issue:: 3
Issue Sort Value:: 2013-0083-0003-0000
Page Start:: 288
Page End:: 290
Publication Date:: 2013-04-19
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/j.1399-0004.2012.01901.x ↗
Languages:: English
ISSNs:: 0009-9163
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3286.287000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 19319.xml