D‐‐phenotype due to RHD‐RHCE hybrid transcript in a case of severe haemolytic disease of newborn with anti‐Rh 17(Hrₒ) antibodies-Reference-Cited by-同舟云学术

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D‐‐phenotype due to RHD‐RHCE hybrid transcript in a case of severe haemolytic disease of newborn with anti‐Rh 17(Hrₒ) antibodies

Published:2021-06-13 Issue:5 Volume:31 Page:383-386
ISSN:0958-7578
Container-title:Transfusion Medicine
language:en
Short-container-title:Transfusion Medicine

Author:

Mani Anila¹^ORCID,Mishra Garima²^ORCID,Kulkarni Swati²,Gupta Debasish¹

Affiliation:

1. Department of Transfusion Medicine Sree Chitra Tirunal Institute for Medical Sciences Thiruvananthapuram Kerala India

2. Department of Transfusion Medicine, ICMR‐National Institute of Immunohematology KEM Hospital Campus, Parel Mumbai Maharashtra India

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/tme.12799

Reference11 articles.

1. A Case Report of a Rare Rh Phenotype: D—

2. The Structure and Function of the Rh Antigen Complex

3. Anti‐Rh17 (anti‐Hr0): a rare diagnostic and management problem;Salamat N;J Pak Med Assoc,2004

4. Molecular genotyping of clinically important blood group antigens in patients with thalassaemia

5. A convenient qualitative and quantitative method to investigateRHD-RHCEhybrid genes

Cited by 3 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. 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

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