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Journal Abstract Search

213 related items for PubMed ID: 15637993

  • 1. [Molecular characteristics of the thalassemia syndrome and prenatal diagnosis in a high risk family].
    Vujić D, Cvorkov--Drazić M, Pavlović S, Bunjevacki G, Popović Z, Puzigaća Z.
    Srp Arh Celok Lek; 2001; 129 Suppl 1():56-8. PubMed ID: 15637993
    [Abstract] [Full Text] [Related]

  • 2. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
    Zhu BS, He J, Zhang J, Zeng XH, Su J, Xu XH, Li SY, Chen H, Zhang YH.
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
    [Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis of beta-thalassaemia mutations using the reverse dot blot technique.
    Muralitharan S, Srivastava A, Shaji RV, Mathai M, Srivastava VM, Dennison D, Lu CY, Krishnamoorthy R.
    Natl Med J India; 1996 Feb; 9(2):70-1. PubMed ID: 8857041
    [Abstract] [Full Text] [Related]

  • 4. Analysis of cosegregation of intragenic DNA sequence variations as markers of maternal cell contamination in prenatal diagnosis of β-thalassemia.
    Saadi AV, Girisha KM, Gopinath PM, Satyamoorthy K.
    Transl Res; 2011 Mar; 157(3):150-5. PubMed ID: 21316031
    [Abstract] [Full Text] [Related]

  • 5. Beta-thalassemia in association with a new delta-chain hemoglobin variant [delta116(g18)Arg-->Leu]: implications for carrier screening and prenatal diagnosis.
    Waye JS, Patterson M, Walker L, Eng B, Nakamura LM, Lafferty JD, Yong SL, Wu JK, Chui DH.
    Am J Hematol; 2003 Nov; 74(3):179-81. PubMed ID: 14587045
    [Abstract] [Full Text] [Related]

  • 6. A novel beta-delta globin gene fusion, anti-Lepore Hong Kong, leads to overexpression of delta globin chain and a mild thalassaemia intermedia phenotype when co-inherited with beta(0)-thalassaemia.
    So CC, Chan AY, Tsang ST, Lee AC, Au WY, Ma ES, Chan LC.
    Br J Haematol; 2007 Jan; 136(1):158-62. PubMed ID: 17222202
    [Abstract] [Full Text] [Related]

  • 7. [Diagnostic strategy of beta-thalassemic mutation in a Tunisian family, application in prenatal diagnosis].
    Khelil AH, Laradi S, Ferchichi S, Carion N, Béjaoui M, Saad A, Chaieb A, Miled A, Ben Chibani J, Perrin P.
    Ann Biol Clin (Paris); 2003 Jan; 61(2):229-33. PubMed ID: 12702481
    [Abstract] [Full Text] [Related]

  • 8. [A rare thalassemia intermedia case caused by co-existence of Hb H disease (--(SEA)/-alpha(4.2)) and beta-thalassemia major (beta (CD17A)>T/beta (IVS2-654C)>T): implications for prenatal diagnosis].
    Li Q, Li LY, Mo QH.
    Nan Fang Yi Ke Da Xue Xue Bao; 2008 Jan; 28(1):16-9. PubMed ID: 18227017
    [Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis of beta-thalassemia in Egypt: implementing accurate high-tech methods did not reflect much on the outcome.
    Elgawhary S, Elbaradie Sahar MY, Rashad WM, Mosaad M, Abdalla MA, Ezzat G, Wali YA, Elbeshlawy A.
    Pediatr Hematol Oncol; 2008 Sep; 25(6):541-8. PubMed ID: 18728973
    [Abstract] [Full Text] [Related]

  • 10. A simple non radioactive method for detecting beta-thalassemia/hbe disease: application to prenatal diagnosis.
    Fucharoen S, Fucharoen G, Ratanasiri T, Jetsrisuparb A, Fukumaki Y.
    Southeast Asian J Trop Med Public Health; 1995 Sep; 26 Suppl 1():278-81. PubMed ID: 8629124
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis of beta-thalassemia in the West Bank and Gaza.
    Ayesh SK, Al-Sharef WA, Nassar SM, Thawabteh NA, Abu-Libdeh BY.
    Saudi Med J; 2005 Nov; 26(11):1771-6. PubMed ID: 16311664
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13.
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  • 14. 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 May; 32(2):138-44. PubMed ID: 16096209
    [Abstract] [Full Text] [Related]

  • 15. Variable haematological and clinical presentation of β-thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian population.
    Italia K, Sawant P, Surve R, Wadia M, Nadkarni A, Ghosh K, Colah R.
    Eur J Haematol; 2012 Aug; 89(2):160-4. PubMed ID: 22690826
    [Abstract] [Full Text] [Related]

  • 16. Profile of beta-thalassemia in eastern India and its prenatal diagnosis.
    Bandyopadhyay A, Bandyopadhyay S, Basak J, Mondal BC, Sarkar AA, Majumdar S, Das MK, Chandra S, Mukhopadhyay A, Sanghamita M, Ghosh K, Dasgupta UB.
    Prenat Diagn; 2004 Dec 15; 24(12):992-6. PubMed ID: 15614841
    [Abstract] [Full Text] [Related]

  • 17. [A case of prenatal diagnosis of beta-thalassemia by polymerase chain reaction].
    Kolesnikova TN, Moliaka IuK, Surin VL, Luk'ianenko AV, Asanov AIu, Tagiev AF, Solov'ev GIa.
    Genetika; 1992 Dec 15; 28(12):130-4. PubMed ID: 1363470
    [Abstract] [Full Text] [Related]

  • 18. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A, Picanço I, Gomes S, Miranda A, Coucelo M, Seuanes F, Seixas MT, Romão L, Faustino P.
    Eur J Haematol; 2007 Nov 15; 79(5):422-8. PubMed ID: 17916081
    [Abstract] [Full Text] [Related]

  • 19. Accurate and rapid prenatal diagnosis of the most frequent East Mediterranean beta-thalassemia mutations.
    Naja RP, Kaspar H, Shbaklo H, Chakar N, Makhoul NJ, Zalloua PA.
    Am J Hematol; 2004 Apr 15; 75(4):220-4. PubMed ID: 15054814
    [Abstract] [Full Text] [Related]

  • 20. A double heterozygote for (deltabeta)0-thalassemia and codons 41/42 (-TTCT) behaves as a homozygote for the frameshift mutation in a Chinese family.
    Liao C, Feng Q, Li J, Huang Y, Li D.
    Hemoglobin; 2007 Apr 15; 31(3):397-400. PubMed ID: 17654080
    [Abstract] [Full Text] [Related]

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