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Journal Abstract Search

292 related items for PubMed ID: 15967770

  • 1.
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  • 2. The spectrum of beta-globin gene mutations in children with beta-thalassaemia major from Kota Kinabalu, Sabah, Malaysia.
    Thong MK, Soo TL.
    Singapore Med J; 2005 Jul; 46(7):340-3. PubMed ID: 15968446
    [Abstract] [Full Text] [Related]

  • 3. Detection of beta-globin gene mutations among Kelantan Malay thalassaemia patients by polymerase chain reaction restriction fragment length polymorphism.
    Rozitah R, Nizam MZ, Nur Shafawati AR, Nor Atifah MA, Dewi M, Kannan TP, Ariffin N, Norsarwany M, Setianingsih I, Harahap A, Zilfalil BA.
    Singapore Med J; 2008 Dec; 49(12):1046-9. PubMed ID: 19122960
    [Abstract] [Full Text] [Related]

  • 4. Establishment of prenatal diagnosis for beta-thalassaemia: a step towards its control in a developing country.
    Garewal G, Das R, Jaur J, Marwaha RK, Gupta I.
    Ann Hum Biol; 2005 Dec; 32(2):138-44. PubMed ID: 16096209
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  • 5. Prenatal diagnosis of beta-thalassaemia: experience in a developing country.
    Saxena R, Jain PK, Thomas E, Verma IC.
    Prenat Diagn; 1998 Jan; 18(1):1-7. PubMed ID: 9483634
    [Abstract] [Full Text] [Related]

  • 6. Prenatal diagnosis and control strategies for beta-thalassaemia on the Indian subcontinent.
    Varawalla NY.
    Natl Med J India; 1992 Jan; 5(4):157-61. PubMed ID: 1304300
    [Abstract] [Full Text] [Related]

  • 7. 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 Jan; 31(1):63-9. PubMed ID: 17365006
    [Abstract] [Full Text] [Related]

  • 8. Spectrum of beta-thalassemia mutations and their association with allelic sequence polymorphisms at the beta-globin gene cluster in an Eastern Indian population.
    Kukreti R, Dash D, E VK, Chakravarty S, Das SK, De M, Talukder G.
    Am J Hematol; 2002 Aug; 70(4):269-77. PubMed ID: 12210807
    [Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis of beta-thalassaemia by reverse dot-blot hybridization.
    Winichagoon P, Saechan V, Sripanich R, Nopparatana C, Kanokpongsakdi S, Maggio A, Fucharoen S.
    Prenat Diagn; 1999 May; 19(5):428-35. PubMed ID: 10360511
    [Abstract] [Full Text] [Related]

  • 10. Spectrum of beta-thalassaemia mutations in transfusion dependent thalassaemia patients: practical implications in prenatal diagnosis.
    George E, George R, Ariffin WA, Mokhtar AB, Azman ZA, Sivagengei K.
    Med J Malaysia; 1993 Sep; 48(3):325-9. PubMed ID: 8183146
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  • 13. A widely applicable strategy for single cell genotyping of beta-thalassaemia mutations using DGGE analysis: application to preimplantation genetic diagnosis.
    Vrettou C, Palmer G, Kanavakis E, Tzetis M, Antoniadi T, Mastrominas M, Traeger-Synodinos J.
    Prenat Diagn; 1999 Dec; 19(13):1209-16. PubMed ID: 10660957
    [Abstract] [Full Text] [Related]

  • 14. The use of the amplification refractory mutation system (arms) in the detection of rare beta-thalassemia mutations in the Malays and Chinese in Malaysia.
    Chan Yoke Fan, Tan Kim Lian, Wong Yean Ching, Wee Yong Chui, Yap Sook Fan, Tan Jin Ai Mary Anne.
    Southeast Asian J Trop Med Public Health; 2001 Dec; 32(4):872-9. PubMed ID: 12041567
    [Abstract] [Full Text] [Related]

  • 15. Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.
    Darwish HM, El-Khatib FF, Ayesh S.
    Hemoglobin; 2005 Dec; 29(2):119-32. PubMed ID: 15921164
    [Abstract] [Full Text] [Related]

  • 16. The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.
    Basak AN.
    Hemoglobin; 2007 Dec; 31(2):233-41. PubMed ID: 17486506
    [Abstract] [Full Text] [Related]

  • 17. The molecular analysis of beta-thalassemia mutations in Lorestan Province, Iran.
    Kiani AA, Mortazavi Y, Zeinali S, Shirkhani Y.
    Hemoglobin; 2007 Dec; 31(3):343-9. PubMed ID: 17654071
    [Abstract] [Full Text] [Related]

  • 18. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians.
    Garewal G, Das R, Awasthi A, Ahluwalia J, Marwaha RK.
    Eur J Haematol; 2007 Nov; 79(5):417-21. PubMed ID: 17900295
    [Abstract] [Full Text] [Related]

  • 19. Characterisation and confirmation of rare beta-thalassaemia mutations in the Malay, Chinese and Indian ethnic groups in Malaysia.
    Tan JA, Chin PS, Wong YC, Tan KL, Chan LL, George E.
    Pathology; 2006 Oct; 38(5):437-41. PubMed ID: 17008283
    [Abstract] [Full Text] [Related]

  • 20. The spectrum of beta-thalassemia mutations in Malays in Singapore and Kelantan.
    Abdullah WA, Jamaluddin NB, Kham SK, Tan JA.
    Southeast Asian J Trop Med Public Health; 1996 Mar; 27(1):164-8. PubMed ID: 9031421
    [Abstract] [Full Text] [Related]

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