Severe hemolytic disease of the fetus and newborn due to allo-anti-D in a patient with a partial DEL phenotype arising from the variant allele described asRHD*148+1T (RHD*01EL.31)-Reference-Cited by-同舟云学术

Severe hemolytic disease of the fetus and newborn due to allo-anti-D in a patient with a partial DEL phenotype arising from the variant allele described asRHD*148+1T (RHD*01EL.31)

Published:2018-09-17 Issue:10 Volume:58 Page:2260-2264
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Turley Elona¹²,McGowan Eunike C.³^ORCID,Hyland Catherine A.³,Schoeman Elizna M.³^ORCID,Flower Robert L.³,Skoll Amanda⁴,Delisle Marie-France⁴,Nelson Tanya⁵,Clarke Gwen¹⁶,Au Nicholas⁷

Affiliation:

1. Department of Laboratory Medicine and Pathology; University of Alberta

2. Alberta Health Services; Edmonton Alberta Canada

3. Research and Development; Australian Red Cross Blood Service, Kelvin Grove; Brisbane Queensland Australia

4. Maternal Fetal Medicine, Department of Obstetrics and Gynecology; BC Women's Hospital, University of British Columbia; Vancouver British Columbia Canada

5. Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine; BC Children's Hospital and BC Women's Hospital, University of British Columbia; Vancouver British Columbia Canada

6. Canadian Blood Services; Edmonton Alberta Canada

7. Hematopathology, Department of Pathology and Laboratory Medicine; BC Children's Hospital and BC Women's Hospital, University of British Columbia; Vancouver British Columbia Canada

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/trf.14944/fullpdf

Reference16 articles.

1. Prenatal determination of fetal RhD type by DNA amplification;Bennett;N Engl J Med,1993

2. Molecular cloning of RhD cDNA derived from a gene present in RhD-positive, but not RhD-negative individuals;Arce;Blood,1993

3. http://www.isbtweb.org/fileadmin/user_upload/Working_parties/WP_on_Red_Cell_Immunogenetics_and/004_RHD_weak_D_and_Del_alleles_v5.0_180207.pdf

4. Evaluation of targeted exome sequencing for 28 protein-based blood group systems, including the homologous gene systems, for blood group genotyping;Schoeman;Transfusion,2017

5. Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting;Schoeman;Transfusion,2018

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hemolytic disease of the fetus and newborn—a perspective of immunohematology;Hematology, Transfusion and Cell Therapy;2024-08

2. Serological analysis of Rh antigens: how far can we go?;Annals of Blood;2023-12

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

4. Serology and molecular biology of DEL: a narrative review;Annals of Blood;2023-09

5. Asian‐type DEL (RHD*DEL1) with an allo‐anti‐D: A paradoxical observation in a healthy multiparous woman;Transfusion;2023-07-19