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Article

PCR screening for common weak D types shows different distributions in three Central European populations.

Transfusion - 1 Jan 2001

Müller T H, Wagner F F, Trockenbacher A, Eicher N I, Flegel W A, Schönitzer D, Schunter F, Gassner C

Abstract excerpt

BACKGROUND: DNA sequencing showed RHD mutations for all weak D phenotypes investigated in a study from Southwestern Germany. Molecular classification of weak D offers a more reliable basis than serotyping and is relevant for optimal D transfusion strategies. STUDY DESIGN AND METHODS: Sequence-specific primers were designed to detect weak D types 1 to 5 and the partial D phenotype HMi in a modular set for...

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Source

Identifiers

PMID: 11161244
DOI: 10.1046/j.1537-2995.2001.41010045.x

Genes

RHD

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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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