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Journal Abstract Search

168 related items for PubMed ID: 2640144

  • 1. [Detection of sickle cell gene by analysis of amplified DNA sequences].
    Huang SZ, Sheng M, Zhao JQ, Qiu XK, Zeng YT, Wang QS, He MX, Zhu JM, Liu WP, Li WW.
    Yi Chuan Xue Bao; 1989; 16(6):475-82. PubMed ID: 2640144
    [Abstract] [Full Text] [Related]

  • 2. Molecular analysis of Iranian families with sickle cell disease.
    Ayatollahi M, Zakerinia M, Haghshenas M.
    J Trop Pediatr; 2005 Jun; 51(3):136-40. PubMed ID: 15831669
    [Abstract] [Full Text] [Related]

  • 3. Analysis of sickle cell gene using polymerase chain reaction & restriction enzyme Bsu 361.
    Husain SM, Kalavathi P, Anandaraj MP.
    Indian J Med Res; 1995 Jun; 101():273-6. PubMed ID: 7672839
    [Abstract] [Full Text] [Related]

  • 4. [Application of the polymerase chain reaction to the diagnosis of sickle cell anemia in Venezuela].
    Martínez J, Blanco Z, Hakshaw P, Moreno N.
    Sangre (Barc); 1998 Feb; 43(1):63-6. PubMed ID: 9577183
    [Abstract] [Full Text] [Related]

  • 5. A family study of HbS in a Malay family by molecular analysis.
    Hafiza A, Noor HH, Noor FA, Azlin I, Ainoon O.
    Malays J Pathol; 2010 Dec; 32(2):137-41. PubMed ID: 21329186
    [Abstract] [Full Text] [Related]

  • 6. Rapid prenatal diagnosis of sickle cell anemia by a new method of DNA analysis.
    Embury SH, Scharf SJ, Saiki RK, Gholson MA, Golbus M, Arnheim N, Erlich HA.
    N Engl J Med; 1987 Mar 12; 316(11):656-61. PubMed ID: 3821796
    [Abstract] [Full Text] [Related]

  • 7. Molecular exclusion of haemoglobin SD disease by prenatal diagnosis.
    Fodor FH, Eng CM.
    Prenat Diagn; 1999 Jan 12; 19(1):58-60. PubMed ID: 10073909
    [Abstract] [Full Text] [Related]

  • 8. Heterogeneity of DNA fragments associated with the sickle-globin gene.
    Feldenzer J, Mears JG, Burns AL, Natta C, Bank A.
    J Clin Invest; 1979 Sep 12; 64(3):751-5. PubMed ID: 468989
    [Abstract] [Full Text] [Related]

  • 9. Use of the amplification refractory mutation system (ARMS) in the study of HbS in predynastic Egyptian remains.
    Marin A, Cerutti N, Massa ER.
    Boll Soc Ital Biol Sper; 1999 Sep 12; 75(5-6):27-30. PubMed ID: 11148985
    [Abstract] [Full Text] [Related]

  • 10. Sequence of the -530 region of the beta-globin gene of sickle cell anemia patients with the Arabian haplotype.
    Zeng FY, Rodgers GP, Huang SZ, Schechter AN, Salamah M, Perrine S, Berg PE.
    Hum Mutat; 1994 Sep 12; 3(2):163-5. PubMed ID: 8199597
    [No Abstract] [Full Text] [Related]

  • 11. DNAase I hypersensitive site 3' to the beta-globin gene cluster contains a TAA insertion specific for beta(S)-Benin haplotype.
    Bordin S, Crespi VG, Duarte AS, Bassères DS, Melo MB, Vieira AP, Saad ST, Costa FF.
    Haematologica; 2002 Mar 12; 87(3):246-9. PubMed ID: 11869935
    [Abstract] [Full Text] [Related]

  • 12. Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb beta-globin gene deletion.
    Andersson BA, Wering ME, Luo HY, Basran RK, Steinberg MH, Smith HP, Chui DH.
    Eur J Haematol; 2007 Jan 12; 78(1):82-5. PubMed ID: 17038017
    [Abstract] [Full Text] [Related]

  • 13. The real-time polymerase chain reaction.
    Kubista M, Andrade JM, Bengtsson M, Forootan A, Jonák J, Lind K, Sindelka R, Sjöback R, Sjögreen B, Strömbom L, Ståhlberg A, Zoric N.
    Mol Aspects Med; 2006 Jan 12; 27(2-3):95-125. PubMed ID: 16460794
    [Abstract] [Full Text] [Related]

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  • 15. Preimplantation genetic diagnosis for beta-thalassemia using single-cell DNA analysis for codons 17 and 26 of beta-globin gene.
    Nasri NW, Jamal AR, Abdullah NC, Razi ZR, Mokhtar NM.
    Arch Med Res; 2009 Jan 12; 40(1):1-9. PubMed ID: 19064120
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  • 17. Prenatal diagnosis of unusual hemoglobinopathies.
    Kim JH, Lebo RV, Cai SP, Su X, Chung JH, Mentzer WC, Golbus MS.
    Am J Med Genet; 1994 Mar 01; 50(1):15-20. PubMed ID: 8160747
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  • 19. Real-time PCR for single-cell genotyping in sickle cell and thalassemia syndromes as a rapid, accurate, reliable, and widely applicable protocol for preimplantation genetic diagnosis.
    Vrettou C, Traeger-Synodinos J, Tzetis M, Palmer G, Sofocleous C, Kanavakis E.
    Hum Mutat; 2004 May 01; 23(5):513-21. PubMed ID: 15108284
    [Abstract] [Full Text] [Related]

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