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Article

[Para-Bombay phenotype caused by combined heterozygote of two bases deletion on fut1 alleles].

Zhongguo shi yan xue ye xue za zhi - 1 Feb 2011

Ma Kan-Rong, Tao Shu-Dan, Lan Xiao-Fei, Hong Xiao-Zhen, Xu Xian-Guo, Zhu Fa-Ming, Lü Hang-Jun, Yan Li-Xing

Abstract excerpt

This study was purposed to investigate the molecular basis of a para-Bombay phenotype for screening and identification of rare blood group. ABO and H phenotypes of the proband were identified by serological techniques. The exon 6 to exon 7 of ABO gene and full coding region of α-1,2-fucosyltransferase (fut1) gene of the proband were analyzed by polymerase chain reaction and direct sequencing of the amplified...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 21362257

Genes

ABO

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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[Para-Bombay phenotype caused by combined heterozygote of two bases deletion on fut1 alleles].PMID 21362257Read ↗

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Genetic and mechanistic evaluation of an individual with para-Bombay phenotype associated with a compound heterozygote comprising two novel FUT1 variants.Semantic proximity Read ↗

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Analysis of the molecular mechanism and pedigree investigation of para-Bombay phenotype caused by combined mutations at position h649 and h768 of FUT1 gene.Semantic proximity Read ↗

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