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Journal Abstract Search

146 related items for PubMed ID: 26182339

  • 1. First Detection of a Splice Acceptor Site β-Thalassemia Mutation: IVS-I-130 (HBB: c.93-1G > C) in a Chinese Patient.
    He S, Zhang Q, Zheng C, Wei Y, Tang Y, Chen Q, Chen S.
    Hemoglobin; 2015; 39(4):290-1. PubMed ID: 26182339
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Mild β(+)-thalassemia associated with two linked sequence variants: IVS-II-839 (T>C) and IVS-II-844 (C>A).
    Waye JS, Eng B, Hellens L, Hohenadel BA, Nakamura LM, Walker L.
    Hemoglobin; 2013; 37(4):378-86. PubMed ID: 23651435
    [Abstract] [Full Text] [Related]

  • 4. Combination of Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G] and β0-Thalassemia in a Chinese Patient with β-Thalassemia Intermedia.
    Li Y, Yan JM, Zhou JY, Lu YC, Li DZ.
    Hemoglobin; 2017 Jan; 41(1):47-49. PubMed ID: 28366026
    [Abstract] [Full Text] [Related]

  • 5. First Description of a β-Thalassemia Mutation, -86 (C > G) (HBB: c.-136C > G), in a Chinese Family.
    He S, Qin Q, Yi S, Zhou W, Deng J, Zheng C, Chen B.
    Hemoglobin; 2015 Jan; 39(6):448-50. PubMed ID: 26291972
    [Abstract] [Full Text] [Related]

  • 6. 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
    [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
    [Abstract] [Full Text] [Related]

  • 8. Splice Acceptor Mutation [HBB:c.93-2A > T] in a Patient with Hb S/β0-Thalassemia.
    Waye JS, Hanna M, Nakamura L, Walker L, Eng B, Nfonsam LE.
    Hemoglobin; 2024 Mar; 48(2):116-117. PubMed ID: 38360540
    [Abstract] [Full Text] [Related]

  • 9. Characterization of the IVS-II-821 (A>C) (HBB: c.316-30A>C) Mutation in a β-Thalassemia Phenotype in Iran.
    Azimi A, Nejati P, Tahmasebi S, Alimoradi S, Alibakhshi R.
    Hemoglobin; 2019 Jan; 43(1):23-26. PubMed ID: 31146650
    [Abstract] [Full Text] [Related]

  • 10. Description of a rare β-globin gene mutation, IVS-II-848 (C>A) (HBB: c.316-3C>A) in association with IVS-I-1 (G>A) (HBB: c.92 + 1G>A), observed in a Syrian family: a case report.
    Shoujaa A, Mukhalalaty Y, Murad H, Al-Quobaili F.
    Hemoglobin; 2019 Jan; 43(4-5):283-285. PubMed ID: 31718331
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Molecular Scanning of β-Thalassemia in the Southern Region of Central Java, Indonesia; a Step Towards a Local Prevention Program.
    Rujito L, Basalamah M, Mulatsih S, Sofro AS.
    Hemoglobin; 2015 Jan; 39(5):330-3. PubMed ID: 26291967
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. 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 Jul; 38(4):292-4. PubMed ID: 24986053
    [Abstract] [Full Text] [Related]

  • 15. Compound Heterozygosity for a Novel Mutation Codon 104 (-A) (HBB: c.313delA) and Codons 41/42 (-CTTT) (HBB: c.126_129delCTTT) Leading to β-Thalassemia Major in a Chinese Family.
    Qiu Y, Huang Y, Chen P, Wei S, Su Q, Zhang Z, Yang Z, Ye L, Huang J, Shen X, Mo W.
    Hemoglobin; 2020 Nov; 44(6):402-405. PubMed ID: 33198537
    [Abstract] [Full Text] [Related]

  • 16. Hb S/β-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics.
    Belisário AR, Carneiro-Proietti AB, Sabino EC, Araújo A, Loureiro P, Máximo C, Flor-Park MV, Rodrigues DDOW, Ozahata MC, McClure C, Mota RA, Gomes Moura IC, Custer B, Kelly S, Recipient Epidemiology and Donor Evaluation Study (REDS-III) International Component Brazil.
    Hemoglobin; 2020 Jan; 44(1):1-9. PubMed ID: 32172616
    [Abstract] [Full Text] [Related]

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

  • 18. A Novel β-Thalassemia Mutation [IVS-I-6 (T>G), HBB: c.92+6T>G] in a Chinese Family.
    Luo H, Zou Y, Liu Y.
    Hemoglobin; 2020 Jan; 44(1):55-57. PubMed ID: 31939318
    [Abstract] [Full Text] [Related]

  • 19. Updated Molecular Spectrum of β-Thalassemia Mutations in Duhok Province, Northern Iraq: Ethnic Variation and the Impact of Immigration.
    Atroshi SD, Al-Allawi NAS, Eissa AA.
    Hemoglobin; 2021 Jul; 45(4):239-244. PubMed ID: 34794358
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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