α‑thalassaemia combined with hereditary spherocytosis in the same patient-Reference-Cited by-同舟云学术

α‑thalassaemia combined with hereditary spherocytosis in the same patient

Published:2017-11-28 Issue: Volume: Page:
ISSN:1792-0981
Container-title:Experimental and Therapeutic Medicine
language:
Short-container-title:Exp Ther Med

Author:

Li Xiaohong¹,Liao Lin¹,Deng Xuelian¹,Huang Jian¹,Deng Zengfu²,Wei Hongying³,Mo Wuning¹,Lin Faquan¹

Affiliation:

1. Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region 530021, P.R. China

2. Department of Clinical Laboratory, First Affiliated Hospital of Guangxi University of Traditional Chinese Medicine, Nanning, Guangxi Zhuang Autonomous Region 530021, P.R. China

3. Department of Paediatrics, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region 530021, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Immunology and Microbiology (miscellaneous),General Medicine

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1. The coincidence of beta‐thalassemia and hereditary spherocytosis: A case report and literature review;Clinical Case Reports;2024-06

2. Peripheral Blood Smear Findings in 2 Patients With Coexisting Thalassemia and Hereditary Spherocytosis;Journal of Pediatric Hematology/Oncology;2022-09-13

3. The diagnostic protocol for hereditary spherocytosis‐2021 update;Journal of Clinical Laboratory Analysis;2021-10-24

4. A tetranucleotide deletion in the ANK1 gene causes hereditary spherocytosis; a case of misdiagnosis;Gene;2020-02