Pages that link to "Q77324096"

The following pages link to Point mutations and deletion responsible for the Bombay H null and the Reunion H weak blood groups (Q77324096):

Displaying 10 items.

• Molecular genetic analysis of para-Bombay phenotypes in Chinese: a novel non-functional FUT1 allele is identified (Q28205528) (← links)
• DNA sequence variation of the human ABO-secretor locus ( FUT2) in New Guinean populations: possible early human migration from Africa. (Q33194079) (← links)
• Cutaneous chronic graft-versus-host disease does not have the abnormal endothelial phenotype or vascular rarefaction characteristic of systemic sclerosis (Q33480033) (← links)
• Two Novel α 1,2-Fucosyltransferase Alleles in an H-Deficient Phenotype Individual (Q34687191) (← links)
• Identification of a rare blood group, "Bombay (Oh) phenotype," in Bhuyan tribe of Northwestern Orissa, India (Q35199813) (← links)
• Genomic analysis of para-Bombay individuals in south-eastern China: the possibility of linkage and disequilibrium between FUT1 and FUT2. (Q36187375) (← links)
• Human intestinal organoids express histo-blood group antigens, bind norovirus VLPs, and support limited norovirus replication (Q41925105) (← links)
• Molecular genotyping and frequencies of A1, A2, B, O1 and O2 alleles of the ABO blood group system in a Kuwaiti population (Q45114545) (← links)
• A novel FUT1 allele was identified in a Chinese individual with para‐Bombay phenotype (Q50524887) (← links)
• The polymorphisms of fucosyltransferases (Q73847070) (← links)