Human RhDel Is Caused by a Deletion of 1,013 bp Between Introns 8 and 9 Including Exon 9 of RHD Gene-Reference-Cited by-同舟云学术

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Human RhDel Is Caused by a Deletion of 1,013 bp Between Introns 8 and 9 Including Exon 9 of RHD Gene

Published:1998-10-01 Issue:7 Volume:92 Page:2602-2604
ISSN:1528-0020
Container-title:Blood
language:en
Short-container-title:

Author:

Chang Jan-Gowth¹,Wang Jyh-Chwan¹,Yang Tzu-Yao¹,Tsan Kun-Wu¹,Shih Mu-Ching²,Peng Ching-Tien³,Tsai Chang-Hai³

Affiliation:

1. Department of Internal Medicine; Department of Medical Research; Division of Molecular Medicine; Mackay Memorial Hospital; Taipei, Taiwan

2. Department of Laboratory Medicine; Changhua Christain Hospital; Changhua, Taiwan

3. Department of Medical Research and Pediatrics; China Medical College Hospital; Taichung, Taiwan

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/92/7/2602/1449562/2602.pdf

Reference5 articles.

1. A D variant, Del?;Okubo;Transfusion,1984

2. A recombination hot spot in the Rh gene revealed by analysis of unrelated donors with the rare D—phenotype.;Kemp;Am J Hum Genet,1996

3. Molecular definition of red cell Rh haplotypes by tightly linked Sph I RFLPs.;Huang;Am J Hum Genet,1996

4. Aberrant FHIT transcripts in cancerous and corresponding non-cancerous lesions of the digestive tract.;Chen;Int J Cancer,1997

5. Rapid molecular diagnosis of hemoglobin variants by RT-PCR of reticulocytes mRNA and direct sequencing.;Liu;Hemoglobin,1992

Cited by 48 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. Transfusion management of Africans with RHD variants in China;Transfusion Clinique et Biologique;2023-05

2. DEL in China: the D antigen among serologic RhD-negative individuals;Journal of Translational Medicine;2021-10-20

3. Effects ofRHDgene polymorphisms on distinguishing weak D or DEL from RhD− in blood donation in a Chinese population;Molecular Genetics & Genomic Medicine;2019-04-05

4. A DEL phenotype attributed toRHDExon 9 sequence deletion: slipped-strand mispairing and blood group polymorphisms;Transfusion;2017-12-06

5. Two large deletions extending beyond either end of the RHD gene and their red cell phenotypes;Journal of Human Genetics;2017-11-16

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