Associated Papers
Genomic alterations linked to recurrence risk in high-grade serous ovarian cancer revealed by deep targeted sequencing.
Park YH et al.
Scientific Reports, 2025
41413429 (PubMed )
Supplement: 41598_2025_26481_MOESM2_ESM.xlsx › Supplementary_Table_S2
Correlation of genetic alterations by whole-exome sequencing with clinical outcomes of glioblastoma patients from the Lebanese population.
Saadeh FS et al.
Plos One, 2020
33237934 (PubMed )
Supplement: pone.0242793.s003.xlsx › Sheet1
A novel c.1664G > T(p.Gly555Val) mutation in the KEL gene encoding the Kmod phenotype.
Horikawa T et al.
Transfusion, 2019
Molecular Basis of KELnull Phenotype in Brazilians.
Boturão-Neto E et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2015
Expansion of the Kell blood group system: two new high-prevalence antigens and two novel K0 (Kellnull ) phenotypes.
Lomas-Francis C et al.
Transfusion, 2013
Genetic diversity of KELnull and KELel: a nationwide Austrian survey.
Körmöczi GF et al.
Transfusion, 2007
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