Identification of a novel variant c.761C>T on ABO*B.01 gene in ABO glycosyltransferases associated with Bweak phenotype
Hang Lei, Hui Zhang, Liujun Guo, Dong Xiang, Xuefeng Wang, Xi Liu, Xiaohong Cai - 11/08/2023
Genetic diversity of Gerbich alleles in Brazilians reveals an unexpected prevalence of the GE:?2,?3,4 phenotype
Carine Prisco Arnoni, Nayara Morais Silva, Flavia Sant'Anna Silva, Rafael Martins Parreira, Tati - 08/08/2023
A novel nonsense variant in RHAG underlies a Nordic Rhnull phenotype
Asa Hellberg, Mirjana Grujic Arsenovic, Ingvild Hausberg Sorvoll, Norbert Lubenow, Inna Sareneva, Ka - 02/06/2023
Secretor status of blood group O mothers is associated with development of ABO haemolytic disease in the newborn
Grethe Risum Krog, Henriette Lorenzen, Frederik Banch Clausen, Morten Hanefeld Dziegiel - 09/03/2023
Fatal haemolytic transfusion reaction due to anti-Ena and identification of a novel GYPA c.295delG variant in a Thai family
Ploymanee du Swanwood, Gengis H. Lopez, Emthip de Morakot, Brett Wilson, Glenda M. Millard, Sunisa O - 14/09/2022
The Crawford variant as a cause of RhD typing discrepancies in blood banks: A case report
Sussan Barrera, Margarita Bolívar, Ayda Rodríguez, Adriana Urbina - 18/08/2022
A rare case of clinically significant naturally occurring anti-Cw reported in a healthy male donor
Prashant Pandey, Supriya Kumari, Divya Setya, Mukesh Kumar Singh - 07/08/2022
What is the optimal pretransfusion testing interval for multi-transfused patients? The University Hospital of Brest experience
C. Le Niger, C. Andre - 22/02/2022
Perinatal risk factors associated with severity of haemolytic disease of the foetus and newborn due to Rhc maternal-foetal incompatibility: A retrospective cohort study
Loriane Franchinard, Emeline Maisonneuve, Stéphanie Friszer, Cécile Toly Ndour, Stéphanie Huguet Jac - 07/11/2021