Recurrent mutations in the deafness geneGJB2 (connexin 26) in British Asian families. Issue 8 (1st August 2001)

Record Type:: Journal Article
Title:: Recurrent mutations in the deafness geneGJB2 (connexin 26) in British Asian families. Issue 8 (1st August 2001)
Main Title:: Recurrent mutations in the deafness geneGJB2 (connexin 26) in British Asian families
Authors:: Rickard, Sarah
Kelsell, David P
Sirimana, Tony
Rajput, Kaukab
MacArdle, Breege
Bitner-Glindzicz, Maria
Abstract:
Is Part Of:: Journal of medical genetics. Volume 38:Issue 8(2001)
Journal:: Journal of medical genetics
Issue:: Volume 38:Issue 8(2001)
Issue Display:: Volume 38, Issue 8 (2001)
Year:: 2001
Volume:: 38
Issue:: 8
Issue Sort Value:: 2001-0038-0008-0000
Page Start:: 530
Page End:: 533
Publication Date:: 2001-08-01
Subjects:: Medical genetics -- Periodicals
616.042
Journal URLs:: http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jmg.38.8.530 ↗
Languages:: English
ISSNs:: 1468-6244
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 18156.xml