Varaico: Literature-Extracted Genetic Variants

Gene:RHD
Variant:p.T32insFs
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RHD

NM_016124.6:p.T32insFs

Associated Papers

Investigation of discrepancies obtained during 15 years of non-invasive fetal RHD genotyping in apparent serologic RhD-negative pregnant women.

Dufour P et al.

Prenatal Diagnosis, 2022

A practical and effective strategy in East Asia to prevent anti-D alloimmunization in patients by C/c phenotyping of serologic RhD-negative blood donors.

Ito S et al.

Ejhaem, 2021

Performance evaluation study of ID RHD XT, a new genotyping assay for the detection of high-prevalence RhD negative and weak D types.

Molano A et al.

Vox Sanguinis, 2018

The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes.

Scott SA et al.

Transfusion, 2014

Strategy for managing maternal variant RHD alleles in Rhesus D negative obstetric populations during fetal RHD genotyping.

Hyland CA et al.

Prenatal Diagnosis, 2014

New RHCE variant alleles encoding the D- - phenotype.

Ochoa-Garay G et al.

Transfusion, 2013

Alloimmunization of patients by blood units harboring distinct DEL variants.

St-Louis M et al.

Immunohematology, 2013

[Genotyping of 21,000 blood donors in Quebec and RHD analysis].

St-Louis M et al.

Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2010

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."