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BackgroundThe D– phenotype is mainly caused by the complete deletion of the RHD gene in Caucasians. However, a plethora of allelic variants have been described among D– individuals from different ethnic groups.
Study Design and MethodsA cohort of 1314 routine serologically D– samples from white Argentineans was studied by molecular methods.
ResultsAmong the 1314 D– samples, 2.1% showed RHD‐specific...
BACKGROUND: The serologic assignment of the RhD status may be hindered in patients with weak D expression. A comprehensive study of RHD alleles occurring in the mixed population of Argentina is necessary to evaluate the most suitable DNA typing strategy.
STUDY DESIGN AND METHODS: A total of 18,379 patients from two stratified groups, Group 1 (G1; public hospital) and Group 2 (G2; private laboratory),...
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