A Pediatric Patient with a Complicated History of Sickle Cell Trait-Reference-Cited by-同舟云学术

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A Pediatric Patient with a Complicated History of Sickle Cell Trait

Published:2022-10-04 Issue:10 Volume:68 Page:1245-1248
ISSN:0009-9147
Container-title:Clinical Chemistry
language:en
Short-container-title:

Author:

Nedelcu Elena¹²,Wiencek Joesph R²^ORCID,Pierre Christina C³^ORCID

Affiliation:

1. Department of Laboratory Medicine, University of California San Francisco , San Francisco, CA , USA

2. Pathology, Microbiology and Immunology, Vanderbilt University Medical Center , Nashville, TN , USA

3. Department of Pathology and Laboratory Medicine, Penn Medicine Lancaster General Hospital , Lancaster, PA , USA

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

Link

https://academic.oup.com/clinchem/article-pdf/68/10/1245/46354914/hvac139.pdf

Reference10 articles.

1. Sickle cell disease;Kato;Nat Rev Dis Primers,2018

2. Screening for sickle cell disease in newborns: a systematic review;Runkel;Syst Rev,2020

3. The carrier state for sickle cell disease is not completely harmless;Xu;Haematologica,2019

4. Clinical utility of the addition of molecular genetic testing to newborn screening for sickle cell anemia;Jain;Front Med,2021

5. Sickle cell disease in a patient with sickle cell trait and compound heterozygosity for hemoglobin S and hemoglobin Quebec-Chori;Witkowska;N Engl J Med,1991

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