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American Journal of Medical Genetics|November 1, 1992
Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafnessW Reardon, S Roberts, P D Phelps, et al.
Human Genetics|December 1, 1986
Localisation of the gene for Hunter syndrome on the long arm of X chromosomeM Upadhyaya, M Sarfarazi, J S Bamforth, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Clinical findings in 33 subjects with large supernumerary marker(15) chromosomes and 3 subjects with triplication of 15q11-q13N R Dennis, M W M Veltman, R Thompson, et al.
Journal of Clinical Pathology|August 29, 2006
Current research priorities in chronic fatigue syndrome/myalgic encephalomyelitis: disease mechanisms, a diagnostic test and specific treatmentsJ R Kerr, P Christian, A Hodgetts, et al.
Blood|August 15, 1994
Differentiation-linked changes in tyrosine phosphorylation, functional activity, and gene expression downstream from the granulocyte-macrophage colony-stimulating factor receptorP J Roberts, A Khwaja, A K Lie, et al.
Cell|July 27, 1990
Molecular cloning and characterization of the human double-stranded RNA-activated protein kinase induced by interferonE Meurs, K Chong, J Galabru, et al.
The British Journal of Nutrition|January 25, 2013
A consideration of biomarkers to be used for evaluation of inflammation in human nutritional studiesP C Calder, N Ahluwalia, R Albers, et al.
Lancet (London, England)|February 24, 1990
Development of antibodies to unprotected glycosylation sites on recombinant human GM-CSFJ G Gribben, S Devereux, N S Thomas, et al.
Molecular Syndromology|April 19, 2012
Novel Tandem Duplication in Exon 1 of the SNURF/SNRPN Gene in a Child with Transient Excessive Eating Behaviour and Weight GainS Naik, N S Thomas, J H Davies, et al.
Cytogenetic and Genome Research|November 9, 2005
Molecular investigation of a dicentric 13;17 chromosome found in a 21-week gestation fetus with multiple congenital abnormalitiesA E Cockwell, V K Maloney, N S Thomas, et al.
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