Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Zhen-Min Ren"'
Publikováno v:
Hematology, Vol 28, Iss 1 (2023)
ABSTRACTBackground In China, conventional genetic testing methods can only detect common thalassemia variants. Accurate detection of rare thalassemia is crucial for clinical diagnosis, especially for children that need long-term blood transfusion. Th
Externí odkaz:
https://doaj.org/article/795900d62e6b442c90034168e62ed6c4
Publikováno v:
Hemoglobin. 46:160-163
With the development of sequencing technology, more and more rare thalassemia types have been found. In this article, we found a novel Hb H disease combined with glucose-6-phosphate dehydrogenase (G6PD) deficiency through whole genome sequencing (WGS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfc117ce75a6258771c070263498e4c6
https://doi.org/10.1080/03630269.2022.2070072
https://doi.org/10.1080/03630269.2022.2070072
Autor:
Zhen-Min, Ren, Chang-Gang, Li, Gang, Xu, Juan, Huang, Zhen-Hu, Lin, Mei-Zhu, Luo, Shi-Yang, Chen, Yun-Sheng, Chen
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 28(1)
to explore the value of capillary electrophoresis in screening β- thalassemia of children, and to establish the cutoff values of HbA2 and HbF in our laboratory.The data of hemoglobin capillary electrophoresis and genetic diagnosis of β- thalassemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::609643d0c008acb4d3c11c096d5aeb61
https://pubmed.ncbi.nlm.nih.gov/32027282
https://pubmed.ncbi.nlm.nih.gov/32027282
Publikováno v:
Zhongguo Dang Dai Er Ke Za Zhi
OBJECTIVE: To investigate the serum level of soluble transferrin receptor (sTfR) and its association with the degree of anemia in children with hemoglobin H (HbH) disease. METHODS: A total of 55 children with HbH disease were enrolled as the HbH grou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ccc365b1bb4922936e548d00ba238445
https://pubmed.ncbi.nlm.nih.gov/31506149
https://pubmed.ncbi.nlm.nih.gov/31506149
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 27(4)
To analyze the genotype and hematological characteristics of children with αβ-thalassemia in Shenzhen area of China.The erythrocyte parameters and hemoglobin components of the children were determined by blood routine examination and capillary elec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::188ae93aabf6b2971adb16b784352e1a
https://pubmed.ncbi.nlm.nih.gov/31418385
https://pubmed.ncbi.nlm.nih.gov/31418385