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 *

130 related articles for article (PubMed ID: 1517110)

  • 1. A novel frameshift mutation: deletion of C in codons 74/75 of the beta-globin gene causes beta zero-thalassemia in a Turkish patient.
    Başak AN; Ozer A; Ozçelik H; Kirdar B; Gürgey A
    Hemoglobin; 1992; 16(4):309-12. PubMed ID: 1517110
    [No Abstract]   [Full Text] [Related]  

  • 2. Identification of five rare mutations including a novel frameshift mutation causing beta zero-thalassemia in Thai patients with beta zero-thalassemia/hemoglobin E disease.
    Winichagoon P; Fucharoen S; Wilairat P; Chihara K; Fukumaki Y; Wasi P
    Biochim Biophys Acta; 1992 Aug; 1139(4):280-6. PubMed ID: 1515453
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of two novel beta zero-thalassemia mutations in a Filipino family: frameshift codon 67 (-TG) and a beta-globin gene deletion.
    Eng B; Chui DH; Saunderson J; Olivieri NF; Waye JS
    Hum Mutat; 1993; 2(5):375-9. PubMed ID: 8257991
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A new frameshift mutation, insertion of ATCT, at codon 48 in the beta-globin gene causes beta-thalassemia in an Indian proband.
    Jain PK; Dozy AM; Verma IC; Chehab FF
    Hum Mutat; 1994; 3(4):397-8. PubMed ID: 8081396
    [No Abstract]   [Full Text] [Related]  

  • 5. Nonsense and frameshift mutations in beta 0-thalassemia detected in cloned beta-globin genes.
    Orkin SH; Goff SC
    J Biol Chem; 1981 Oct; 256(19):9782-4. PubMed ID: 6985481
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel frameshift mutation (+A) at codon 18 of the beta-globin gene associated with high persistence of fetal hemoglobin phenotype and deltabeta-thalassemia.
    Feriotto G; Salvatori F; Finotti A; Breveglieri G; Venturi M; Zuccato C; Bianchi N; Borgatti M; Lampronti I; Mancini I; Massei F; Favre C; Gambari R
    Acta Haematol; 2008; 119(1):28-37. PubMed ID: 18230963
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A newly discovered frameshift at codons 120-121 (+A) of the beta gene is not associated with a dominant form of beta-thalassemia.
    Hopmeier P; Krugluger W; Gu LH; Smetanina NS; Huisman TH
    Blood; 1996 Jun; 87(12):5393-4. PubMed ID: 8652860
    [No Abstract]   [Full Text] [Related]  

  • 8. A novel deletion in a Turkish beta-thalassemia patient detected by DGGE and direct sequencing: FSC 22-24 (-7 bp).
    Ozçelik H; Başak AN; Tüzmen S; Kirdar B; Akar N
    Hemoglobin; 1993 Aug; 17(4):387-91. PubMed ID: 8226099
    [No Abstract]   [Full Text] [Related]  

  • 9. Frameshift codon 5 [Fsc-5 (-CT)] thalassemia; a novel mutation detected in a Greek patient.
    Kollia P; Gonzalez-Redondo JM; Stoming TA; Loukopoulos D; Politis C; Huisman TH
    Hemoglobin; 1989; 13(6):597-604. PubMed ID: 2606727
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A new codon 31 (-C) mutant resulting in beta zero-thalassemia.
    Lin LI; Lin KS; Lin KH
    Proc Natl Sci Counc Repub China B; 1992 Jan; 16(1):6-9. PubMed ID: 1631246
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A Novel Frameshift Mutation at Codons 138/139 (HBB: c.417_418insT) on the β-Globin Gene Leads to β-Thalassemia.
    Jiang F; Huang LY; Chen GL; Zhou JY; Xie XM; Li DZ
    Hemoglobin; 2017 Jan; 41(1):59-60. PubMed ID: 28460555
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characterization of beta-thalassemia mutations among the Japanese.
    Hattori Y; Yamane A; Yamashiro Y; Matsuno Y; Yamamoto K; Yamamoto K; Ohba Y; Miyaji T
    Hemoglobin; 1989; 13(7-8):657-70. PubMed ID: 2634667
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemia.
    Oner R; Agarwal S; Dimovski AJ; Efremov GD; Petkov GH; Altay C; Gurgey A; Huisman TH
    Hemoglobin; 1991; 15(1-2):67-76. PubMed ID: 1717406
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Beta zero-thalassemia in a Thai family is caused by a 3.4 kb deletion including the entire beta-globin gene.
    Sanguansermsri T; Pape M; Laig M; Hundrieser J; Flatz G
    Hemoglobin; 1990; 14(2):157-68. PubMed ID: 2272839
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Two new beta0-thalassemic mutations: a deletion (-CC) at codon 142 or overlapping codons 142-143, and an insertion (+T) at codon 45 or overlapping codons 44-45/45-46 of the beta-globin gene.
    Lacan P; Aubry M; Couprie N; Francina A
    Hemoglobin; 2007; 31(2):159-65. PubMed ID: 17486497
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Beta-thalassemia intermedia in Turkey.
    Altay C; Gürgey A
    Ann N Y Acad Sci; 1990; 612():81-9. PubMed ID: 2291577
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Study of beta-Thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian Thalassemia patients.
    El-Gawhary S; El-Shafie S; Niazi M; Aziz M; El-Beshlawy A
    Hemoglobin; 2007; 31(1):63-9. PubMed ID: 17365006
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A 4 base pair TGAT insertion at codon 116 of the beta globin gene causes beta0-thalassemia.
    Frischknecht H; Kiewitz R; Schmugge M
    Haematologica; 2005 Nov; 90 Suppl():ECR20. PubMed ID: 16266911
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Beta-thalassemia due to frameshifts at codons 5, 6, 8, and 8/9; hematological observations in heterozygotes.
    Agarwal S; Oner R; Kutlar F; Huisman TH
    Hemoglobin; 1990; 14(4):471-5. PubMed ID: 1704359
    [No Abstract]   [Full Text] [Related]  

  • 20. beta-Thalassemia due to a deletion of the nucleotide which is substituted in the beta S-globin gene.
    Kazazian HH; Orkin SH; Boehm CD; Sexton JP; Antonarakis SE
    Am J Hum Genet; 1983 Sep; 35(5):1028-33. PubMed ID: 6310991
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.