Clinical phenotypes of three children with sickle cell disease caused by <scp>HbS</scp> /Sicilian (δβ) <sup>0</sup> ‐thalassemia deletion-Reference-Cited by-同舟云学术

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Clinical phenotypes of three children with sickle cell disease caused by HbS /Sicilian (δβ) ⁰ ‐thalassemia deletion

Published:2022-01-26 Issue:4 Volume:97 Page:
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:American J Hematol

Author:

Aygun Banu¹,Bello Adriana²,Thompson Alexis A.³,Davis Lance⁴,Sun Yanan⁴,Luo Hong‐yuan⁴,Cui Shuaiying⁴^ORCID,Chui David H. K.⁴^ORCID

Affiliation:

1. Cohen Children's Medical Center of New York New Hyde Park New York USA

2. Centro Médico Docente la Trinidad Caracas Venezuela

3. The Ann and Robert H. Lurie Children's Hospital of Chicago Northwestern University Feinberg School of Medicine Chicago Illinois USA

4. Boston Medical Center Boston University School of Medicine Boston Massachusetts USA

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajh.26470

Reference10 articles.

1. Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin

2. Rapid detection of a 13.4-kb deletion causing delta beta thalassemia in an Egyptian family by polymerase chain reaction [letter]

3. Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations

4. The Thalassaemia Syndromes

5. Disorders of Hemoglobin

Cited by 2 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. Scalable noninvasive amplicon-based precision sequencing (SNAPseq) for genetic diagnosis and screening of β-thalassemia and sickle cell disease using a next-generation sequencing platform;Frontiers in Molecular Biosciences;2023-12-13

2. Microcytic Anemia: An Insidious Presentation of Sickle Cell Beta+ Thalassemia, a Rare Sickle Cell Variant;Cureus;2022-03-18

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