First report of the rare RhCE‐depleted D‐‐phenotype in sixteen people of Iranian origin-Reference-Cited by-同舟云学术

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First report of the rare RhCE‐depleted D‐‐phenotype in sixteen people of Iranian origin

Published:2019-02-19 Issue:3 Volume:114 Page:256-261
ISSN:0042-9007
Container-title:Vox Sanguinis
language:en
Short-container-title:Vox Sang

Author:

Shahverdi Ehsan¹²^ORCID,Moghaddam Mostafa¹,Abolghasemi Hassan³

Affiliation:

1. Blood Transfusion Research Center High Institute for Research and Education in Transfusion Medicine Tehran Iran

2. Department of Transfusion Medicine Institute of Immunology and Transfusion Medicine University Medicine Greifswald Greifswald Germany

3. Pediatric Congenital Hematologic Disorders Research Center Shahid Beheshti University of Medical Sciences Tehran Iran

Publisher

Wiley

Subject

Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/vox.12738

Reference20 articles.

1. Maternal ABO-mismatched blood for intrauterine transfusion of severe hemolytic disease of the newborn due to anti-Rh17

2. Molecular genetics of RH;Flegel W;Vox Sang,1999

3. A Probable Deletion in a Human Rh Chromosome

4. A possible deletion in a human Rh chromosome: a serological and genetical study;Race R;Br J Exp Pathol,1951

5. Ten Homozygous –D–Individuals in One Italian Village

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1. Management of severe hemolytic disease of the fetus and newborn due to maternal anti‐Rh17: Using incompatible blood;Pediatric Blood & Cancer;2024-08

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

3. Challenges in blood transfusion caused by anti-Hr0: A rare case of D-- Phenotype in Asia Abstract;Egyptian Journal of Medical Human Genetics;2024-05-22

4. The use of pluripotent stem cells to generate diagnostic tools for transfusion medicine;Blood;2022-10-13

5. Ethical Issues and Management of Fetal Hemolytic Anemia Caused by Anti-Rh17 in a Multipara with Rare –D– Phenotype;Transfusion Medicine and Hemotherapy;2021

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