These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

65 related articles for article (PubMed ID: 35150653)

  • 1. A novel 4.9 Kb deletion at beta-globin gene is identified by the third-generation sequencing: Case report from Baoan, China.
    Chen X; Luo M; Pan L; Huang Y; Yan Z; Shen K; Mai G; Liang H; Li J; Chen Y; Xiong L
    Clin Chim Acta; 2022 Apr; 529():10-16. PubMed ID: 35150653
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of a novel 107 kb deletion in the alpha-globin gene cluster using third-generation sequencing.
    Li Y; Liang L; Guo W; Wu X; Qin T; Tian M
    Clin Biochem; 2023 Mar; 113():36-39. PubMed ID: 36572139
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Case report: Identification of a novel triplication of alpha-globin gene by the third-generation sequencing: pedigree analysis and genetic diagnosis.
    Chen Y; Xie T; Ma M; Yang J; Lv Y; Dong X
    Hematology; 2023 Dec; 28(1):2277571. PubMed ID: 38059617
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Third-generation sequencing identified a novel complex variant in a patient with rare alpha-thalassemia.
    Zhou C; Du Y; Zhang H; Wei X; Li R; Wang J
    BMC Pediatr; 2024 May; 24(1):330. PubMed ID: 38741052
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of a novel 10.3 kb deletion causing α
    Xu R; Li H; Yi S; Du J; Jin J; Qin Y; Jiang Y; Gao T; Zhang C; Yi M; Liu Y; Meng W; Li J; Song J
    Clin Biochem; 2023 Mar; 113():64-69. PubMed ID: 36610469
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of two novel β-globin gene mutations HBB: exon3del, HBB: c.-81A>C.
    Cao Y; Luo J
    Hematology; 2023 Dec; 28(1):2265723. PubMed ID: 37815396
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Case report: A novel 10.8-kb deletion identified in the β-globin gene through the long-read sequencing technology in a Chinese family with abnormal hemoglobin testing results.
    Shao M; Wan Y; Cao W; Yang J; Cui D; Ma M; Hu W
    Front Med (Lausanne); 2023; 10():1192279. PubMed ID: 37521358
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of a novel 91.5 kb-deletion (αα)
    Xu L; Chen M; Zheng J; Zhang S; Zhang M; Chen L; He Q; Guo D; Lin N; Huang H
    J Matern Fetal Neonatal Med; 2023 Dec; 36(2):2254890. PubMed ID: 37673790
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The diagnosis and molecular analysis of a novel 27.2 kb deletion causing α
    Wang G; Zou S; Li J; Wang X; Wu H; Tao Z; Zhang Q; Xu X; Zhou Y
    Clin Biochem; 2023 Jun; 116():20-23. PubMed ID: 36878345
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prevalence Rate of Thalassemia Carriers among Individuals with Microcytosis or Hypochromia in Portugal.
    Santos D; Barreto M; Kislaya I; Mendonça J; P Machado M; Lopes P; Matias Dias C; Faustino P
    Acta Med Port; 2023 Jul; 36(7-8):467-474. PubMed ID: 36898140
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detecting rare thalassemia in children with anemia using third-generation sequencing.
    Ren ZM; Li WJ; Xing ZH; Fu XY; Zhang JY; Chen YS; Li DF
    Hematology; 2023 Dec; 28(1):2241226. PubMed ID: 37548329
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Case report: Long-read sequencing identified a novel 14.9-kb deletion of the α-globin gene locus in a family with α-thalassemia in China.
    Yuan Y; Zhou X; Deng J; Zhu Q; Peng Z; Chen L; Zou Y; Mao A; Meng W; Ma M; Wu H
    Front Genet; 2023; 14():1156071. PubMed ID: 36936435
    [No Abstract]   [Full Text] [Related]  

  • 13. Identification of a Novel 16.8Kb Deletion of the α-Globin Gene Cluster by Third-Generation Sequencing.
    Jiang F; Huang S; Liu T; Wang J; Zhou J; Zuo L; Li J; Li R; Liao C; Li D
    Hemoglobin; 2024 Jul; ():1-6. PubMed ID: 39007770
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of four novel large deletions and complex variants in the α-globin locus in Chinese population.
    Bao X; Wang J; Qin D; Yao C; Liang J; Liang K; Zeng Y; Du L
    Hum Genomics; 2023 Apr; 17(1):38. PubMed ID: 37098594
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel Promoter Mutation (
    Pan L; Tian P; Chen S; Zhang R
    Hemoglobin; 2023 Jan; 47(1):21-24. PubMed ID: 36866928
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Utilization of multiple genetic methods for prenatal diagnosis of rare thalassemia variants.
    Jiang F; Zhou J; Zuo L; Tang X; Li J; Li F; Yang T; Qu Y; Wan J; Liao C; Li D
    Front Genet; 2023; 14():1208102. PubMed ID: 37529778
    [No Abstract]   [Full Text] [Related]  

  • 17. Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families.
    Bao X; Qin D; Wang J; Chen J; Yao C; Liang J; Liang K; Wang Y; Wang Y; Du L; Yin A
    Hum Genomics; 2023 Dec; 17(1):111. PubMed ID: 38062488
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular spectrum and prevalence of thalassemia investigated by third-generation sequencing in the Dongguan region of Guangdong Province, Southern China.
    Lou J; Sun M; Mao A; Liu Y; Zhao Y; Fu Y; Dai Y; Xiong F; Li D; Zhang J; Yan T; Liu Y
    Clin Chim Acta; 2023 Nov; 551():117622. PubMed ID: 37922731
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Alpha-Thalassemia in Southern Italy: Characterization of Five New Deletions Removing the Alpha-Globin Gene Cluster.
    Cardiero G; Musollino G; Prezioso R; Nigro V; Lacerra G
    Int J Mol Sci; 2023 Jan; 24(3):. PubMed ID: 36768900
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of double heterozygous -α
    Liang L; Xiao Y; Guo W; Xie T; Zheng L; Li Y
    Hematology; 2023 Dec; 28(1):2250646. PubMed ID: 37615562
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.