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Article

A null allele caused by a four-base-pair duplication within the RHCE gene encoding a D- - phenotype.

Transfusion - 1 Mar 2021

Chen Qing, Xiao Jianyu, Zhang Min, Huang Chengyin, Li Min, Flegel Willy A, Zhou Xiaoyu

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 33270227
DOI: 10.1111/trf.16211
PMCID: PMC9066653

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A null allele caused by a four-base-pair duplication within the RHCE gene encoding a D- - phenotype.PMID 33270227Read ↗

D-- phenotype caused by a novel RHCE null allele.Semantic proximity Read ↗

RHCE null allele causing D-- phenotype in a Latin-American blood donor.Semantic proximity Read ↗

Rhnull disease: the amorph type results from a novel double mutation in RhCe gene on D-negative background.Semantic proximity Read ↗

A new allele of the Rh gene E.Semantic proximity Read ↗

TWO EXAMPLES OF THE RH GENOTYPE CDE/CDE (RYRY) IN A SWISS FAMILY.Semantic proximity Read ↗

The c.254C>A change (p.Ala85Glu) in RHD causing a weak D phenotype.Semantic proximity Read ↗

THE RH 'DELETION' PHENOTYPES AND THE INFORMATION THEY PROVIDE ABOUT THE RH GENES.Semantic proximity Read ↗

An intron c.149-2632T>A change in RHD is associated with aberrant transcription and very weak D phenotype.Semantic proximity Read ↗

A novel RHCE*Ce710A allele (p.237Asp) in a Japanese patient with weak expression of C and no detectable e.Semantic proximity Read ↗

The RhD- trait in a white patient with the RhCCee phenotype attributed to a four-nucleotide deletion in the RHD gene.Semantic proximity Read ↗

A novel RHD allele caused by c.767 C>T mutation was identified in a Chinese individual.Semantic proximity Read ↗

The novel RHD c.325A>G single nucleotide variation found in Argentineans leads to a partial D phenotype.Semantic proximity Read ↗

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