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Article

Novel RHD variant causing RhD negative phenotype identified in a pregnant woman.

Transfusion - 1 Aug 2022

Pardi Cecilia, Hellberg Åsa, Kapadzha Marieta, Olsson Martin L, Isakson Pauline

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

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Source

Identifiers

PMID: 35834428
DOI: 10.1111/trf.17009

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Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Novel RHD variant causing RhD negative phenotype identified in a pregnant woman.PMID 35834428Read ↗

A novel RHD allele caused by c.687_689delAAG variant.Semantic proximity Read ↗

A new RHD variant allele is caused by a RHD 662C>G mutation.Semantic proximity Read ↗

New RHD variant alleles.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 ↗

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

Identification of a novel c.94dupA mutation in RHD allele.Semantic proximity Read ↗

A novel RHD allele, RHD c.56C>G (p.Thr19Arg), with Del phenotype identified in a Chinese family.Semantic proximity Read ↗

Molecular characterization of 13 new RHD alleles.Semantic proximity Read ↗

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

A novel RHD allele, RHD*1166delA, with D-negative phenotype identified in a Chinese family.Semantic proximity Read ↗

A novel missense mutation (c.221G>C) in RHD gene identified in a Chinese woman.Semantic proximity Read ↗

A new RHD variant allele (RHD Gly339Val) shows weakened D expression compared to RHD Gly339Glu and Gly339Arg mutants.Semantic proximity Read ↗

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