A DEL phenotype attributed toRHDExon 9 sequence deletion: slipped-strand mispairing and blood group polymorphisms-Reference-Cited by-同舟云学术

A DEL phenotype attributed toRHDExon 9 sequence deletion: slipped-strand mispairing and blood group polymorphisms

Published:2017-12-06 Issue:3 Volume:58 Page:685-691
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Lopez Genghis H.¹^ORCID,Turner Robyn M.²,McGowan Eunike C.¹^ORCID,Schoeman Elizna M.¹^ORCID,Scott Stacy A.¹,O'Brien Helen¹^ORCID,Millard Glenda M.¹^ORCID,Roulis Eileen V.¹^ORCID,Allen Amanda J.³,Liew Yew-Wah²,Flower Robert L.¹^ORCID,Hyland Catherine A.¹^ORCID

Affiliation:

1. Research and Development; Clinical Services and Research Division, Australian Red Cross Blood Service; Brisbane Queensland Australia

2. Red Cell Reference Laboratory; Clinical Services and Research Division, Australian Red Cross Blood Service; Brisbane Queensland Australia

3. Medical Services; Clinical Services and Research Division, Australian Red Cross Blood Service; Brisbane Queensland Australia

Funder

Australian Red Cross Blood Service for the provision of blood, blood products, and services to the Australian community

Australian Red Cross Blood Service Human Research Ethics Committee

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/trf.14439/fullpdf

Reference39 articles.

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4. Human RhDel is caused by a deletion of 1,013 bp between introns 8 and 9 including exon 9 of RHD gene;Chang;Blood,1998

5. Molecular background of Rh D-positive, D-negative, D(el) and weak D phenotypes in Chinese;Shao;Vox Sang,2002

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3. DEL variants: review of molecular mechanisms, clinical consequences and molecular testing strategy;Functional & Integrative Genomics;2023-10-16

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