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Transfusion|September 12, 2001
DNA analysis for the Dombrock polymorphismM Rios, K Hue-Roye, A H Lee, et al.Transfusion|January 27, 1999
NOR polyagglutination and Sta glycophorin in one family: relation of NOR polyagglutination to terminal alpha-galactose residues and abnormal glycolipidsG Kuśnierz-Alejska, M Duk, J R Storry, et al.Blood|January 15, 1995
Changes in the blood group Wright antigens are associated with a mutation at amino acid 658 in human erythrocyte band 3: a site of interaction between band 3 and glycophorin A under certain conditionsL J Bruce, S M Ring, D J Anstee, et al.British Journal of Haematology|March 1, 1995
Reactivity with erythroid and non-erythroid tissues of a murine monoclonal antibody to a synthetic peptide having amino acid sequence common to cytoplasmic domain of human glycophorins C and DM J King, C H Holmes, R E Mushens, et al.Immunohematology|October 12, 2010
Consortium for Blood Group Genes (CBGG): 2009 reportG A Denomme, C M Westhoff, L M Castilho, et al.Journal of Telemedicine and Telecare|January 20, 2004
Implementation of videoconferencing to support a managed clinical network in Scotland: lessons learned during the first 18 monthsN Barry, P Campbell, N Reed, et al.Transfusion|October 27, 2004
Altered glycosylation leads to Tr polyagglutinationG R Halverson, A H Lee, R Øyen, et al.Immunohematology|June 16, 2005
Novel molecular basis of an Inab phenotypeK Hue-Roye, V I Powell, G Patel, et al.Journal of the Neurological Sciences|June 1, 1994
A family of McLeod syndrome, masquerading as chorea-acanthocytosisH Takashima, T Sakai, H Iwashita, et al.Transfusion|December 2, 2000
First example of anti-Kx in a person with the McLeod phenotype and without chronic granulomatous diseaseD C Russo, R Oyen, V I Powell, et al.Pageof 23