A null allele caused by a four‐base‐pair duplication within the RHCE gene encoding a D– – phenotype-Reference-Cited by-同舟云学术

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A null allele caused by a four‐base‐pair duplication within the RHCE gene encoding a D– – phenotype

Published:2020-12-03 Issue:3 Volume:61 Page:
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Chen Qing¹²^ORCID,Xiao Jianyu¹,Zhang Min³,Huang Chengyin¹,Li Min²⁴,Flegel Willy A.⁵⁶^ORCID,Zhou Xiaoyu³

Affiliation:

1. Jiangsu Province Blood Center Nanjing China

2. Center for Global Health, School of Public Health Nanjing Medical University Nanjing China

3. Jiangsu Province Hospital The First Affiliated Hospital with Nanjing Medical University Nanjing China

4. Institute of Dermatology Chinese Academy of Medical Science & Peking Union Medical College Nanjing China

5. Department of Transfusion Medicine NIH Clinical Center, National Institutes of Health Bethesda Maryland USA

6. Huazhong University of Science and Technology Wuhan China

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.16211

Reference5 articles.

1. The Outcome of Hemolytic Disease of the Fetus and Newborn Caused by Anti-Rh17 Antibody: Analysis of Three Cases and Review of the Literature

2. Successful management of fetal hemolytic disease due to strong anti-Rh17 with plasma exchange and intrauterine transfusion in a woman with the D−− phenotype

3. Human Blood Groups

4. RhCE protein variants in Southwestern Germany detected by serologic routine testing

5. Short duplication within theRHCEgene associated with an in cis deletedRHDcausing a Rhnullamorph phenotype in an immunized pregnant woman with anti-Rh29

Cited by 2 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. Integrated analyses reveal unexpected complex inversion and recombination in RH genes;Blood Advances;2024-06-13

2. RHCE null allele causing D‐‐ phenotype in a Latin‐American blood donor;Transfusion;2022-02-13

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