Associated Papers
Challenges in the transfusion management of a 15-month-old pediatric patient with Bombay blood group phenotype.
Malhotra S et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2023
Mutational Analysis of Bombay Phenotype in Iranian People: Identification of a Novel FUT1 Allele.
Roshan Mehr F et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion, 2019
Generation of human induced pluripotent stem cells from a Bombay individual: moving towards "universal-donor" red blood cells.
Seifinejad A et al.
Biochemical and Biophysical Research Communications, 2010
Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes.
Storry JR et al.
Transfusion, 2006
Two prevalent h alleles in para-Bombay haplotypes among 250,000 Taiwanese.
Chen DP et al.
Annals of Clinical and Laboratory Science, 2004
The polymorphisms of fucosyltransferases.
Koda Y et al.
Legal Medicine (tokyo, Japan), 2001
Point mutations and deletion responsible for the Bombay H null and the Reunion H weak blood groups.
Fernandez-Mateos P et al.
Vox Sanguinis, 1998
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