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 *

263 related articles for article (PubMed ID: 32811243)

  • 41. Hb Plasencia [α125(H8)Leu→Arg (α2)] is a frequent cause of α+-thalassemia in the Portuguese population.
    Cunha E; Bento C; Oliveira A; Relvas L; Neves J; Gameiro M; Barros C; Araújo A; Macedo A; Rocha P; Costa R; Maia T; Ribeiro ML
    Hemoglobin; 2013; 37(2):183-7. PubMed ID: 23368878
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Molecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (AT
    Lei YL; Sui H; Liu YJ; Pan JJ; Liu YH; Lou JW
    Hemoglobin; 2019; 43(4-5):241-244. PubMed ID: 31690131
    [TBL] [Abstract][Full Text] [Related]  

  • 43. α(+)-Thalassemia trait caused by a frameshift mutation in exon 2 of the α2-globin gene [HBA2 c.244delT].
    Waye JS; Walker L; Eng B
    Hemoglobin; 2012; 36(2):205-7. PubMed ID: 22375514
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a new α-thalassemic hemoglobin variant found in the Iberian Peninsula: report of six cases.
    Bento C; Oliveira AC; Neves J; Gameiro M; Cunha E; Coucelo M; Costa RM; Barbot J; Costa E; Fernández-Lago C; Ribeiro ML
    Hemoglobin; 2012; 36(6):517-25. PubMed ID: 23181747
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Molecular Genetic Analysis of α-Thalassemia in Hamadan Province, West Iran.
    Moradi K; Aznab M; Biglari M; Shafieenia S; Azimi A; Bijari N; Alibakhshi R
    Hemoglobin; 2020 Sep; 44(5):319-324. PubMed ID: 32893703
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Cases Analysis of Hemoglobin H Disease Caused by
    Wang QH; Chen XY; Tang N; Yan TZ; Huang J; Zhong QY; Luo SQ
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2024 Apr; 32(2):520-524. PubMed ID: 38660861
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Two novel α2 gene mutations causing altered amino acid sequences produce a mild (Hb Kinshasa, HBA2: c.428A > T) and severe (HBA2: c.342-345insCC) α-thalassemia phenotype.
    Saller E; Dutly F; Frischknecht H
    Hemoglobin; 2015; 39(2):144-6. PubMed ID: 25786670
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A Novel 31.1 kb α-Thalassemia Deletion (- -
    Rentería-López VM; Perea-Díaz FJ; Rizo-delaTorre LC; Sánchez-López JY; Ibarra-Cortés B
    Hemoglobin; 2017 May; 41(3):180-184. PubMed ID: 28791910
    [TBL] [Abstract][Full Text] [Related]  

  • 49. α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region.
    Al-Riyami AZ; Daar S; Kindi SA; Madhani AA; Wali Y; Rawahi MA; Zadjali SA
    Hemoglobin; 2020 Jan; 44(1):20-26. PubMed ID: 32019385
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Association of Hb A
    Panyasai S; Pornprasert S
    Hemoglobin; 2020 May; 44(3):179-183. PubMed ID: 32482156
    [TBL] [Abstract][Full Text] [Related]  

  • 51. A New Hemoglobin Variant, Hb Natal (
    Efstathiou A; Boutou E; Teli A; Drikos I; Balassopoulou A; Theodoridou S
    Hemoglobin; 2022 Mar; 46(2):132-136. PubMed ID: 36000508
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Identification of nondeletional α-thalassemia in a prenatal screening program by reverse dot-blot in southern China.
    Li J; Li R; Li DZ
    Hemoglobin; 2015; 39(1):42-5. PubMed ID: 25523870
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Severe α-Thalassemia Due to Compound Heterozygosity for Hb Adana (α59 Gly>Asp) (
    Azimi A; Tahmasebi S; Moradi K; Nejati P; Alibakhshi R
    Hemoglobin; 2020 Mar; 44(2):139-142. PubMed ID: 32498570
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [A case with α-thalassemia caused by novel start codon variant in conjunct with right deletion variant of α2-globin gene].
    Chen Y; Wang J; Wang C; Chen S; Feng N; Liu H; Tang X; Zhang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Jan; 38(1):12-14. PubMed ID: 33423249
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Diagnosis of a Family with the Novel -α(21.9) Thalassemia Deletion.
    Long J; Pang W; Sun L; Lao K; Weng X; Ye X; Wu S; Song C; Wei X; Yan S
    Hemoglobin; 2015; 39(6):419-22. PubMed ID: 26479841
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Compound Heterozygosity for HKαα and an in Cis Deletion of Double α Genes Presents as α-Thalassemia Trait.
    Wu MY; Li J; Li SC; Li R; Liao C; Li DZ
    Hemoglobin; 2015; 39(4):256-9. PubMed ID: 26016901
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. First Case of a Compound Heterozygosity for Two Nondeletional α-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze.
    Zhou JY; Yan JM; Li J; Li DZ
    Hemoglobin; 2016 Jun; 40(3):210-2. PubMed ID: 26956449
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A Nested Asymmetric PCR Melting Curve Assay for One-Step Genotyping of Nondeletional α-Thalassemia Mutations.
    Qin J; Xu M; Zhang Q; Wen X; He S; Zhou Y; Liu H; Zhou W
    J Mol Diagn; 2020 Jun; 22(6):794-800. PubMed ID: 32482310
    [TBL] [Abstract][Full Text] [Related]  

  • 60. α(+)-Thalassemia Due to a Frameshift Mutation of the α2-Globin Gene [codons 55/56 (+T) or HBA2: c.168dup].
    Waye JS; Eng B; Hanna M; Hohenadel BA; Nakamura LM; Walker L
    Hemoglobin; 2015; 39(3):209-10. PubMed ID: 25897479
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.