Epidemiology

Variants in mannose-binding lectin and tumour necrosis factor α affect survival in cystic fibrosis
Kitti Buranawuti, Michael P Boyle, Suzanne Cheng, Lori L Steiner, Kathryn McDougal, M Daniele Fallin, Christian Merlo, Pamela L Zeitlin, Beryl J Rosenstein, Peter J Mogayzel, Xinjing Wang, Garry R Cutting

Journal of Medical Genetics Mar 2007, 44 (3) 209-214; DOI: 10.1136/jmg.2006.046318
Common apolipoprotein E polymorphisms and risk of clinical malaria in the Gambia
C Aucan, A J Walley, A V S Hill

Journal of Medical Genetics Jan 2004, 41 (1) 21-24; DOI: 10.1136/jmg.2003.011981
Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery–Dreifuss muscular dystrophy
V Cenni, P Sabatelli, E Mattioli, S Marmiroli, C Capanni, A Ognibene, S Squarzoni, N M Maraldi, G Bonne, M Columbaro, L Merlini, G Lattanzi

Journal of Medical Genetics Mar 2005, 42 (3) 214-220; DOI: 10.1136/jmg.2004.026112
Screening for Fabry disease in high-risk populations: a systematic review
G E Linthorst, M G Bouwman, F A Wijburg, J M F G Aerts, B J H M Poorthuis, C E M Hollak

Journal of Medical Genetics Apr 2010, 47 (4) 217-222; DOI: 10.1136/jmg.2009.072116
Angelman syndrome phenotype associated with mutations inMECP2, a gene encoding a methyl CpG binding protein
Pamela Watson, Graeme Black, Simon Ramsden, Margaret Barrow, Maurice Super, Bronwyn Kerr, Jill Clayton-Smith

Journal of Medical Genetics Apr 2001, 38 (4) 224-228; DOI: 10.1136/jmg.38.4.224
The inheritance of migraine with aura estimated by means of structural equation modelling
Vibeke Ulrich, Morten Gervil, Kirsten O Kyvik, Jes Olesen, Michael B Russell

Journal of Medical Genetics Mar 1999, 36 (3) 225-227; DOI: 10.1136/jmg.36.3.225
Prevalence of mitochondrial DNA mutations in childhood/congenital onset non-syndromal sensorineural hearing impairment
T P Hutchin, K R Thompson, M Parker, V Newton, M Bitner-Glindzicz, R F Mueller

Journal of Medical Genetics Apr 2001, 38 (4) 229-231; DOI: 10.1136/jmg.38.4.229
Loci for primary ciliary dyskinesia map to chromosome 16p12.1-12.2 and 15q13.1-15.1 in Faroe Islands and Israeli Druze genetic isolates
D Jeganathan, R Chodhari, M Meeks, O Færoe, D Smyth, K Nielsen, I Amirav, A S Luder, H Bisgaard, R M Gardiner, E M K Chung, H M Mitchison

Journal of Medical Genetics Mar 2004, 41 (3) 233-240; DOI: 10.1136/jmg.2003.014084
Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairs
M Y M Ng, T Andrew, T D Spector, S Jeffery

Journal of Medical Genetics Mar 2005, 42 (3) 235-239; DOI: 10.1136/jmg.2004.024075
CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTR
Molly B Sheridan, Timothy W Hefferon, Nulang Wang, Christian Merlo, Carlos Milla, Drucy Borowitz, Eric D Green, Peter J Mogayzel, Garry R Cutting

Journal of Medical Genetics Apr 2011, 48 (4) 235-241; DOI: 10.1136/jmg.2010.083287

Main menu

Epidemiology

Pages

Log in using your username and password

Main menu

Log in using your username and password

You are here

Epidemiology

Pages