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Journal of Inherited Metabolic Disease|January 1, 1988
Biochemical basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in nine familiesD T Keough, R B Gordon, J de Jersey, et al.Journal of Clinical Pathology|August 1, 1978
Measurement of ferritin in serum by radioimmunoassayM D Barnett, Y B Gordon, J A Amess, et al.Molecular Genetics and Metabolism|May 3, 2005
Normal HPRT coding region in a male with gout due to HPRT deficiencyPaul A Dawson, Ross B Gordon, Dianne T Keough, et al.Archives of Dermatology|December 17, 2003
Treatment of psoriasis with alefacept: correlation of clinical improvement with reductions of memory T-cell countsKenneth B Gordon, Akshay K Vaishnaw, John O'Gorman, et al.BJOG : an International Journal of Obstetrics and Gynaecology|February 24, 2001
The Ipswich childbirth study: one year follow up of alternative methods used in perineal repairA Grant, B Gordon, C Mackrodat, et al.BMC Cell Biology|March 7, 2001
Alterations in osteoclast morphology following long-term 17beta-estradiol administration in the mouseH E Gruber, I J Puzanov, M Bennett, et al.Transfusion|March 1, 1975
A computerized donor processing system for a regional blood collection centerR W Chambers, J A Lundy, L I Friedman, et al.British Journal of Haematology|November 1, 1995
A simple method for synthesis of B-cell clonospecific probesR J Saal, R B Gordon, R G Cobcroft, et al.Human Genetics|November 1, 1992
A review of the molecular basis of hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiencyD G Sculley, P A Dawson, B T Emmerson, et al.The Journal of Pediatrics|March 10, 2005
Reduced adiponectin and HDL cholesterol without elevated C-reactive protein: clues to the biology of premature atherosclerosis in Hutchinson-Gilford Progeria SyndromeLeslie B Gordon, Ingrid A Harten, Mary Elizabeth Patti, et al.Pageof 146