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 *

137 related articles for article (PubMed ID: 1937477)

  • 1. A rapid and simple electrophoretic method for the detection of mutations involving small insertion or deletion: application to beta-thalassemia.
    Cai SP; Eng B; Kan YW; Chui DH
    Hum Genet; 1991 Oct; 87(6):728-30. PubMed ID: 1937477
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rapid detection of single nucleotide deletions: application to the beta 6 (-A) mutation of the beta-globin gene and to cystic fibrosis.
    Romey MC; Aguilar-Martinez P; Demaille J; Claustres M
    Hum Genet; 1993 Dec; 92(6):627-8. PubMed ID: 8262525
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Molecular nature of beta-thalassemia in Tajikistan: a four base pair deletion in codons 41-42 of the beta-globin gene].
    Kolesnikova TN; Surin VL; Moliaka IuK; Luk'ianenko AV; Tagiev AF; Asanov AIu; Bobokhodzhaev ZM; Solov'ev GIa
    Genetika; 1992 Nov; 28(11):28-33. PubMed ID: 1286798
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A simple electrophoretic procedure for fetal diagnosis of beta-thalassaemia due to short deletions.
    FaĆ  V; Rosatelli MC; Sardu R; Meloni A; Toffoli C; Cao A
    Prenat Diagn; 1992 Nov; 12(11):903-8. PubMed ID: 1494543
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Polymerase chain reaction amplification applied to the direct detection of a 4 bp deletion in the promoter region of the A gamma gene.
    Manca L; Cocco E; Masala B; Gilman JG
    Am J Hematol; 1990 Oct; 35(2):131-3. PubMed ID: 2399905
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detection of alpha-thalassemias by multiplex polymerase chain reaction.
    Bowie LJ; Reddy PL; Nagabhushan M; Sevigny P
    Clin Chem; 1994 Dec; 40(12):2260-6. PubMed ID: 7988013
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Gamma delta beta-thalassemia due to a de novo mutation deleting the 5' beta-globin gene activation-region hypersensitive sites.
    Driscoll MC; Dobkin CS; Alter BP
    Proc Natl Acad Sci U S A; 1989 Oct; 86(19):7470-4. PubMed ID: 2798417
    [TBL] [Abstract][Full Text] [Related]  

  • 8. High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene region.
    Waye JS; Cai SP; Eng B; Clark C; Adams JG; Chui DH; Steinberg MH
    Blood; 1991 Mar; 77(5):1100-3. PubMed ID: 1995096
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular characterization of a novel 10.3 kb deletion causing beta-thalassaemia with unusually high Hb A2.
    Craig JE; Kelly SJ; Barnetson R; Thein SL
    Br J Haematol; 1992 Dec; 82(4):735-44. PubMed ID: 1482661
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of deletions, insertions and single nucleotide substitutions in cloned beta-globin genes and new polymorphic nucleotide substitutions in beta-globin genes in a Japanese population using ribonuclease cleavage at mismatches in RNA:DNA duplexes.
    Hiyama K; Kodaira M; Satoh C
    Mutat Res; 1990 Aug; 231(2):219-31. PubMed ID: 2385239
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoter.
    Coleman MB; Adams JG; Plonczynski MW; Harrell AH; Walker AM; Fairbanks V; Steinberg MH
    Am J Med Sci; 1992 Aug; 304(2):73-8. PubMed ID: 1380206
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characterization of the breakpoint of a 3.5-kb deletion of the beta-globin gene.
    Lynch JR; Brown JM; Best S; Jennings MW; Weatherall DJ
    Genomics; 1991 Jun; 10(2):509-11. PubMed ID: 2071159
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene.
    Losekoot M; Fodde R; Harteveld CL; van Heeren H; Giordano PC; Went LN; Bernini LF
    J Med Genet; 1991 Apr; 28(4):252-5. PubMed ID: 1856830
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?
    Ottolenghi S; Giglioni B; Taramelli R; Comi P; Mazza U; Saglio G; Camaschella C; Izzo P; Cao A; Galanello R; Gimferrer E; Baiget M; Gianni AM
    Proc Natl Acad Sci U S A; 1982 Apr; 79(7):2347-51. PubMed ID: 6179097
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Molecular nature of deletion in beta 0-thalassemia, established using a method of amplification of genomic DNA in vitro].
    Shvarts EI; Gol'tsov AA; Kaboev OK; Bakhlanova IN; Alekseev AN
    Bioorg Khim; 1989 Apr; 15(4):556-9. PubMed ID: 2546567
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The detection of beta-globin gene mutations in beta-thalassemia using oligonucleotide probes and amplified DNA.
    Diaz-Chico JC; Yang KG; Yang KY; Efremov DG; Stoming TA; Huisman TH
    Biochim Biophys Acta; 1988 Jan; 949(1):43-8. PubMed ID: 2825812
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Delta beta-thalassemia in an African-American: identification of the deletion endpoints and PCR-based diagnosis.
    Waye JS; Eng B; Coleman MB; Steinberg MH; Alter BP
    Hemoglobin; 1994 Nov; 18(6):389-99. PubMed ID: 7713743
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The 3' breakpoint of the yunnanese (Agammadeltabeta)0-thalassemia deletion lies in an L1 family sequence: implications for the mechanism of deletion and the reactivation of the Ggamma-globin gene.
    Zhang XQ; Zhang JW
    Hum Genet; 1998 Jul; 103(1):90-5. PubMed ID: 9737783
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of three types of beta zero-thalassemia resulting from a partial deletion of the beta-globin gene.
    Gonzalez-Redondo JM; Kattamis C; Huisman TH
    Hemoglobin; 1989; 13(4):377-92. PubMed ID: 2753736
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Heteroduplex formation: a potential source of genotyping error from PCR products.
    Hatcher SL; Lambert QT; Teplitz RL; Carlson JR
    Prenat Diagn; 1993 Mar; 13(3):171-7. PubMed ID: 8506218
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.