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The use of multiplex ARMS-PCR for mutational analysis of beta-globin gene in consanguineous population of KP Pakistan.

• Authors : Ghalib, Ayesha; Khan, Valeed; Shams, Sumaira

Subjects: SOCIAL impact; CHROMOSOMES; MOLECULAR diagnosis

• Source: Arab Gulf Journal of Scientific Research; 2024, Vol. 42 Issue 3, p714-721, 8p

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Researchers' from University of Swat Report Details of New Studies and Findings in the Area of Thalassemia [Clinical Insights: Prevalence of b-Thalassemia Mutations (IVSI-5, FSC8/9, and CD41/42) in the Swat District].

Subjects: THALASSEMIA; RESEARCH personnel; GENETIC mutation

• Source: Hematology Week; 7/2/2024, p1940-1940, 1p

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Study Data from Aix-Marseille University Update Understanding of Beta Thalassemia (Transfusion Requirements and Complication Rate In Beta-thalassemia Intermedia Due To Heterozygous Ss-globin Gene Mutation and Triplicated Alpha-globin Genes).

Subjects: BETA-Thalassemia; GENETIC mutation; BLOOD diseasesMARSEILLE (France)

• Source: Blood Weekly; 9/14/2023, p639-639, 1p

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Researcher from Medical College and Hospital Details Findings in Beta Thalassemia (Rare mutations in the beta-globin gene and their clinical phenotypes).

Subjects: BETA-Thalassemia; MEDICAL schools; MEDICAL research personnel

• Source: Hematology Week; 6/26/2023, p1253-1253, 1p

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A 6-Year Follow-up of a Chinese Child with Homozygous β0-Thalaasemia and a Heterozygous KLF1 Mutation.

• Authors : Wu, Shao-Min¹ (AUTHOR); Li, Chan¹ (AUTHOR); Huang, Su-Ran¹ (AUTHOR)

Subjects: *GENE expression; *GENETIC counseling; *FACIAL bones

• Source: Hemoglobin. Jan2024, Vol. 48 Issue 1, p60-62. 3p.

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False positive Hb Bart's immunochromatographic strip test for alpha thalassaemia in delta‐beta thalassaemia carriers.

• Authors : Chan, George¹ ; Wong, Jenna¹; Tan, Tina²

Subjects: *THALASSEMIA diagnosis; *CLINICAL pathology; *ALPHA-Thalassemia

• Source: International Journal of Laboratory Hematology. Dec2023, Vol. 45 Issue 6, p984-986. 3p.

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Screening and Diagnosis of Rare Thalassemia Variants.

• Authors : Haishen Tang¹; Yi Xiong¹; Jiaqi Tang¹

Subjects: *THALASSEMIA diagnosis; *RESEARCH funding; *ALPHA-Thalassemia

• Source: Archives of Pathology & Laboratory Medicine. Jan2025, Vol. 149 Issue 1, pe1-e10. 10p.

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β‐thalassemia intermedia mimicking β‐thalassemia trait: The importance of family studies and HBB genotyping in phenotypically ambiguous cases.

• Authors : Singh, Namrata¹; Hira, Jasbir Kaur¹; Chhabra, Sanjeev¹

Subjects: *GENETICS of thalassemia; *THALASSEMIA diagnosis; *HIGH performance liquid chromatography

• Source: International Journal of Laboratory Hematology. Aug2023, Vol. 45 Issue 4, p609-612. 4p.

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Two cases of venous thromboembolism in siblings after splenectomy due to a novel PROC gene mutation.

• Authors : Zhang, Yunfang; Wang, Bo; Bai, Yuxin

Subjects: WARFARIN; THROMBOEMBOLISM risk factors; RISK assessmentCHINA

• Source: Thrombosis Journal; 3/19/2024, Vol. 22 Issue 1, p1-5, 5p

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In situ correction of various β-thalassemia mutations in human hematopoietic stem cells.

• Authors : Yinghong Yang; Lina He; Yingjun Xie

Subjects: HEMATOPOIETIC stem cells; HUMAN stem cells; AUTOTRANSPLANTATION

• Source: Frontiers in Cell & Developmental Biology; 2024, p1-13, 13p

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