BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

266 related articles for article (PubMed ID: 31146650)

  • 1. Characterization of the IVS-II-821 (A>C) (
    Azimi A; Nejati P; Tahmasebi S; Alimoradi S; Alibakhshi R
    Hemoglobin; 2019 Jan; 43(1):23-26. PubMed ID: 31146650
    [TBL] [Abstract][Full Text] [Related]  

  • 2. IVS-II-648/649 (-T) (HBB: c.316-202del) Triggers a Novel β-Thalassemia Phenotype.
    Azimi A; Alibakhshi R; Hayati H; Tahmasebi S; Alimoradi S
    Hemoglobin; 2017 Jan; 41(1):44-46. PubMed ID: 28475449
    [TBL] [Abstract][Full Text] [Related]  

  • 3.
    Tamaddoni A; Khabaz Astaneh S; Tabaripour R; Akhavan-Niaki H
    Hemoglobin; 2019 Jan; 43(1):12-17. PubMed ID: 30747024
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Spectrum of β-Thalassemia Mutations in Hamadan Province, West Iran.
    Alibakhshi R; Moradi K; Aznab M; Azimi A; Shafieenia S; Biglari M
    Hemoglobin; 2019 Jan; 43(1):18-22. PubMed ID: 31096791
    [TBL] [Abstract][Full Text] [Related]  

  • 5. β-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey.
    Guzelgul F; Seydel GS; Aksoy K
    Hemoglobin; 2020 Jul; 44(4):249-253. PubMed ID: 32664780
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Novel Pathogenic β-Thalassemia Mutation Identified at Codon 8 (
    Hasan KN; Sufian A; Mazumder AK; Khaleque MA; Rahman M; Akhteruzzaman S
    Hemoglobin; 2019 May; 43(3):162-165. PubMed ID: 31339392
    [TBL] [Abstract][Full Text] [Related]  

  • 7. First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family.
    Murad H; Moassas F
    Hemoglobin; 2019 Jan; 43(1):66-68. PubMed ID: 30843739
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Two novel mutations in the 3' untranslated region of the beta-globin gene that are associated with the mild phenotype of beta thalassemia.
    Bilgen T; Clark OA; Ozturk Z; Akif Yesilipek M; Keser I
    Int J Lab Hematol; 2013 Feb; 35(1):26-30. PubMed ID: 22862814
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Double Heterozygosity for Hb Durham-N.C. (
    Cannata M; Cassarà F; Vinciguerra M; Licari P; Passarello C; Leto F; Lo Pinto C; Pitrolo L; Ganci R; Maggio A; Giambona A
    Hemoglobin; 2019 May; 43(3):210-213. PubMed ID: 31456457
    [TBL] [Abstract][Full Text] [Related]  

  • 10. First Detection of a Splice Site β-Thalassemia Mutation, IVS-I-6 (T > C) (HBB: c.92 + 6T > C) in a Chinese Family.
    Chen B; Huang P; Yi S; Chen Q; Tang Y; Zhang Q; He S
    Hemoglobin; 2015; 39(3):207-8. PubMed ID: 25856402
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutational Profile of Homozygous β-Thalassemia in Rio de Janeiro, Brazil.
    Carrocini GCS; Venancio LPR; Pessoa VLR; Lobo CLC; Bonini-Domingos CR
    Hemoglobin; 2017 Jan; 41(1):12-15. PubMed ID: 28366028
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Distribution of
    Moradi K; Aznab M; Tahmasebi S; Omidniakan L; Bijari N; Alibakhshi R
    Hemoglobin; 2020 Jul; 44(4):244-248. PubMed ID: 32869674
    [TBL] [Abstract][Full Text] [Related]  

  • 13. IVS-II-16 (G>C) (
    Uçucu S; Karabıyık T; Azik FM
    Hemoglobin; 2021 Jul; 45(4):225-227. PubMed ID: 34396882
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Spectrum of β-Thalassemia Mutations in Siirt Province, Southeastern Turkey.
    Yılmaz S
    Hemoglobin; 2019 May; 43(3):174-181. PubMed ID: 31411089
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia.
    Farashi S; Bayat N; Faramarzi Garous N; Ashki M; Montajabi Niat M; Vakili S; Imanian H; Zeinali S; Najmabadi H; Azarkeivan A
    Hemoglobin; 2015; 39(3):201-6. PubMed ID: 26084319
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular Characterization and Hematological Aspects of Hb E-Myanmar [β26(B8)Glu→Lys and β65(E9)Lys→Asn,
    Satthakarn S; Boonmee S; Panyasai S
    Hemoglobin; 2020 Nov; 44(6):385-390. PubMed ID: 33222574
    [TBL] [Abstract][Full Text] [Related]  

  • 17. β-Thalassemia major resulting from compound heterozygosity for HBB: c.92+2T>C [formerly known as IVS-I-2 (T>C)] and a novel β(0)-thalassemia frameshift mutation: HBB: c.209delG; p.Gly70Valfs*20.
    Kluge ML; Hoyer JD; Swanson KC; Oliveira JL
    Hemoglobin; 2014; 38(4):292-4. PubMed ID: 24986053
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular and phenotype characterization of an elongated β-globin variant produced by HBB:C.313delA.
    Lin W; Zhang Q; Shen Z; Qu X; Wang Q; Wei L; Qiu Y; Yang J; Xu X; Lao J
    Int J Lab Hematol; 2021 Dec; 43(6):1620-1627. PubMed ID: 34271589
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
    Henderson SJ; Timbs AT; McCarthy J; Gallienne AE; Proven M; Rugless MJ; Lopez H; Eglinton J; Dziedzic D; Beardsall M; Khalil MS; Old JM
    Hemoglobin; 2016; 40(2):75-84. PubMed ID: 26635043
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion Mutation.
    Ozkinay F; Onay H; Karaca E; Arslan E; Erturk B; Ece Solmaz A; Tekin IM; Cogulu O; Aydinok Y; Vergin C
    Hemoglobin; 2015; 39(4):230-4. PubMed ID: 26076395
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.