Hemoglobin D in a Patient with Sickle Cell Disease (Genotype HbSS)-Reference-Cited by-同舟云学术

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Hemoglobin D in a Patient with Sickle Cell Disease (Genotype HbSS)

Published:2018-07-01 Issue:1 Volume:3 Page:140-143
ISSN:2475-7241
Container-title:The Journal of Applied Laboratory Medicine
language:en
Short-container-title:

Author:

Rutherford Nicola J¹,Louis Peter C¹,Booth Garrett S¹,Colby Jennifer M¹

Affiliation:

1. Department of Pathology, Microbiology, and Immunology, Vanderbilt University School of Medicine, Nashville TN

Publisher

Oxford University Press (OUP)

Subject

General Medicine

Link

https://academic.oup.com/jalm/article-pdf/3/1/140/42353630/3_3_1_140.pdf

Reference8 articles.

1. Title 21, CFR Parts 610 and 640;Code of Federal Regulations,2010

2. US National Institutes of Health. Evidence-based management of sickle cell disease: expert panel report (EPR), 2014. https://www.nhlbi.nih.gov/sites/default/files/media/docs/sickle-cell-disease-report%20020816_0.pdf (Accessed January 2018).

3. Sickle cell trait in the blood supply;Wiencek;J Appl Lab Med,2017

4. Death following an exchange transfusion with hemoglobin SC blood;Murphy;J Pediatr,1980

Cited by 1 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. Unrecognized Hemoglobin Variants in the Donor Blood Supply Are Detectable in the Transfused Population;American Journal of Clinical Pathology;2020-07-11

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