Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype. Issue 8 (1st August 2002)

Record Type:: Journal Article
Title:: Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype. Issue 8 (1st August 2002)
Main Title:: Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype
Authors:: Faivre, L
Cormier-Daire, V
Lapierre, J M
Colleaux, L
Jacquemont, S
Geneviéve, D
Saunier, P
Munnich, A
Turleau, C
Romana, S
Prieur, M
De Blois, M C
Vekemans, M
Abstract:
Is Part Of:: Journal of medical genetics. Volume 39:Issue 8(2002)
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 8(2002)
Issue Display:: Volume 39, Issue 8 (2002)
Year:: 2002
Volume:: 39
Issue:: 8
Issue Sort Value:: 2002-0039-0008-0000
Page Start:: 594
Page End:: 596
Publication Date:: 2002-08-01
Subjects:: Prader-Willi-like phenotype -- SIM1 gene -- chromosome 6q deletion
Medical genetics -- Periodicals
616.042
Journal URLs:: http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗
DOI:: 10.1136/jmg.39.8.594 ↗
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:: 17950.xml