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American Journal of Human Genetics|August 5, 2000
Identification and analysis of error types in high-throughput genotypingK R Ewen, M Bahlo, S A Treloar, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 15, 2010
Heterogeneity at the HLA-DRB1 allelic variation locus does not influence multiple sclerosis disease severity, brain atrophy or cognitionAnneke Van der Walt, J Stankovich, M Bahlo, et al.
Neurology|September 30, 2009
Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophyA van der Walt, J Stankovich, M Bahlo, et al.
The Journal of Allergy and Clinical Immunology|August 10, 2001
The -590C/T and -34C/T interleukin-4 promoter polymorphisms are not associated with atopic eczema in childhoodK Elliott, E Fitzpatrick, D Hill, et al.
Journal of Thrombosis and Haemostasis : JTH|August 10, 2013
GFI1B mutation causes a bleeding disorder with abnormal platelet functionW S Stevenson, M-C Morel-Kopp, Q Chen, et al.
Clinical Genetics|February 6, 2010
Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutationM S Hildebrand, N P Thorne, C J Bromhead, et al.
Nature Communications|February 5, 2025
Multi-omic spatial effects on high-resolution AI-derived retinal thicknessV E Jackson, Y Wu, R Bonelli, et al.
Genes and Immunity|July 25, 2008
Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in AustraliansJ P Rubio, J Stankovich, J Field, et al.
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