Bombay Phenotype
The Bombay Phenotype is a rare genetic blood type characterized by the absence of the H antigen, the foundational carbohydrate structure required for the expression of A and B antigens, due to homozygous mutations in the FUT1 gene, resulting in individuals phenotypically appearing as type O despite potentially harboring ABO alleles.
68
Publications
2.9K
Citations
271
Authors
114
Institutions
Publications per year
2017–2026
6
Variants
Hh Blood GroupOh Phenotype
Parents
68
1–5 of 68
271
4
h-index
4
h-index
4
h-index
3
h-index
3
h-index
1–5 of 271
114
Kurume University
Kurume, Japan
4 h-index
15 publications
721 citations
National Blood Transfusion Service
Abuja, Nigeria
4 h-index
17 publications
539 citations
Institut National de la Transfusion Sanguine
Paris, France
3 h-index
10 publications
547 citations
German Red Cross
Berlin, Germany
3 h-index
6 publications
244 citations
Inserm
Paris, France
3 h-index
10 publications
672 citations
Africa Society for Blood Transfusion
Durban, South Africa
3 h-index
6 publications
189 citations

Rambam Health Care Campus
Haifa, Israel
3 h-index
5 publications
307 citations

King Edward Memorial Hospital and Seth G.S. Medical College
Mumbai, India
2 h-index
3 publications
98 citations
1–8 of 114
13 publications · 409 citations
11
h-index
11 publications · 285 citations
10
h-index
AJTS · 5 publications · 103 citations
5
h-index
Repository · 4 publications · 110 citations
4
h-index
4 publications · 226 citations
4
h-index
1–5