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Article

Screening for DEL phenotype in RhD negative Indians.

Journal of clinical laboratory analysis - 1 Mar 2018

Kulkarni Swati, Parchure Disha S, Gopalkrishnan Vidya, Madkaikar Manisha

Abstract excerpt

BACKGROUND: DEL phenotype represents a very weak form of D variant detected only by adsorption and elution technique. DEL phenotype individuals mistyped as RhD-negative can lead to alloimmunization after transfusion or pregnancy. Molecular techniques have now been used to identify DEL variants. They are commonly encountered in the East Asian population with RHD(K409K) being the most frequent allele. RHD(M295I) is...

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Share to Sequence Deletion
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 28643361
DOI: 10.1002/jcla.22288
PMCID: PMC6816987

Genes

RHD

Variants

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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