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Article

Mosaicism due to myeloid lineage restricted loss of heterozygosity as cause of spontaneous Rh phenotype splitting.

Blood - 15 Sept 2007

Körmöczi Günther F, Dauber Eva-Maria, Haas Oskar A, Legler Tobias J, Clausen Frederik B, Fritsch Gerhard, Raderer Markus, Buchta Christoph, Petzer Andreas L, Schönitzer Diether, Mayr Wolfgang R, Gassner Christoph

Abstract excerpt

Spontaneous Rh phenotype alteration interferes with pretransfusion and prenatal blood group examinations and may potentially indicate hematologic disease. In this study, the molecular background of this biologic phenomenon was investigated. In 9 patients (3 with hematologic disease), routine RhD...

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Topics

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Share to Mosaicism
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Share to Chromosomes, Human, Pair 1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17537994
DOI: 10.1182/blood-2007-01-068106

Genes

RHCE
RHD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17537994-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

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