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European Journal of Immunology|March 31, 2000
Human intestinal lamina propria and intraepithelial lymphocytes express receptors specific for chemokines induced by inflammationW W Agace, A I Roberts, L Wu, et al.
British Journal of Haematology|May 1, 1996
Idiopathic myelofibrosis in childrenM Sekhar, H G Prentice, U Popat, et al.
The Cochrane Database of Systematic Reviews|April 20, 2007
Methods to increase response rates to postal questionnairesP Edwards, I Roberts, M Clarke, et al.
Cancer Genetics and Cytogenetics|March 25, 2000
Cytogenetics of the chronic myeloid leukemia-derived cell line K562: karyotype clarification by multicolor fluorescence in situ hybridization, comparative genomic hybridization, and locus-specific fluorescence in situ hybridizationS M Gribble, I Roberts, C Grace, et al.
The Cochrane Database of Systematic Reviews|October 21, 2004
Human albumin solution for resuscitation and volume expansion in critically ill patientsP Alderson, F Bunn, C Lefebvre, et al.
The Cochrane Database of Systematic Reviews|March 1, 2002
Human albumin solution for resuscitation and volume expansion in critically ill patientsP Alderson, F Bunn, C Lefebvre, et al.
Child: Care, Health and Development|April 26, 2006
Out-of-home day care for families living in a disadvantaged area of London: economic evaluation alongside a RCTR Mujica Mota, P K Lorgelly, M Mugford, et al.
Blood|July 27, 2001
Simultaneous fetal cell identification and diagnosis by epsilon-globin chain immunophenotyping and chromosomal fluorescence in situ hybridizationM Choolani, H O'Donnell, C Campagnoli, et al.
Health Technology Assessment (Winchester, England)|August 10, 2004
The Social Support and Family Health Study: a randomised controlled trial and economic evaluation of two alternative forms of postnatal support for mothers living in disadvantaged inner-city areasM Wiggins, A Oakley, I Roberts, et al.
British Journal of Haematology|June 1, 1996
Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutationsI Dokal, A Chase, N V Morgan, et al.
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