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527 related items for PubMed ID: 8710774

  • 1. Prenatal diagnosis of cystic fibrosis in a highly heterogeneous population.
    Casals T, Gimenez J, Ramos MD, Nunes V, Estivill X.
    Prenat Diagn; 1996 Mar; 16(3):215-22. PubMed ID: 8710774
    [Abstract] [Full Text] [Related]

  • 2. Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations. The Biomed CF Mutation Analysis Consortium.
    Estivill X, Bancells C, Ramos C.
    Hum Mutat; 1997 Mar; 10(2):135-54. PubMed ID: 9259197
    [Abstract] [Full Text] [Related]

  • 3. [Characterization of 3 microsatellites of the cystic fibrosis gene in Argentine families].
    Visich AA, Barreiro CZ, Chertkoff LP.
    Medicina (B Aires); 2001 Mar; 61(1):23-7. PubMed ID: 11265619
    [Abstract] [Full Text] [Related]

  • 4. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
    Alibakhshi R, Kianishirazi R, Cassiman JJ, Zamani M, Cuppens H.
    J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673
    [Abstract] [Full Text] [Related]

  • 5. Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis.
    Moutou C, Gardes N, Viville S.
    Eur J Hum Genet; 2002 Apr; 10(4):231-8. PubMed ID: 12032730
    [Abstract] [Full Text] [Related]

  • 6. Analysis of linkage disequilibrium between different cystic fibrosis mutations and three intragenic microsatellites in the Italian population.
    Russo MP, Romeo G, Devoto M, Barbujani G, Cabrini G, Giunta A, D'Alcamo E, Leoni G, Sangiuolo F, Magnani C.
    Hum Mutat; 1995 Apr; 5(1):23-7. PubMed ID: 7537148
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  • 9. [Clinical and molecular genetic study of cystic fibrosis in the 5th Region of Chile].
    Molina G, González FJ, Cave R, Cornejo de M, Navarro S, Deglin M, Milinarsky A, Carvallo de P.
    Rev Med Chil; 2002 Aug; 130(8):850-8. PubMed ID: 12360792
    [Abstract] [Full Text] [Related]

  • 10. First study of CF mutations in the CFTR gene of Iranian patients: detection of DeltaF508, G542X, W1282X, A120T, R117H, and R347H mutations.
    Jalalirad M, Houshmand M, Mirfakhraie R, Goharbari MH, Mirzajani F.
    J Trop Pediatr; 2004 Dec; 50(6):359-61. PubMed ID: 15537723
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  • 12. [Prenatal molecular diagnosis of cystic fibrosis. Report of 3 cases].
    Morales-Machín A, Borjas-Fajardo L, Pineda-Del Villar L, Prieto-Carrasquero M, González S, Gutiérrez M, Delgado-Luengo W, Alvarez F, Barrera-Saldaña H.
    Invest Clin; 1997 Sep; 38(3):145-53. PubMed ID: 9376420
    [Abstract] [Full Text] [Related]

  • 13. Mutational spectrum of cystic fibrosis patients from Córdoba province and its zone of influence: implications of molecular diagnosis in Argentina.
    Ramírez AM, Ramos MD, Jiménez J, Ghio A, de Botelli MM, Rezzónico CA, Marqués I, Pereyro S, Casals T, de Kremer RD.
    Mol Genet Metab; 2006 Apr; 87(4):370-5. PubMed ID: 16423550
    [Abstract] [Full Text] [Related]

  • 14. Spectrum of mutations in the CFTR gene in cystic fibrosis patients of Spanish ancestry.
    Alonso MJ, Heine-Suñer D, Calvo M, Rosell J, Giménez J, Ramos MD, Telleria JJ, Palacio A, Estivill X, Casals T.
    Ann Hum Genet; 2007 Mar; 71(Pt 2):194-201. PubMed ID: 17331079
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  • 15. Prenatal diagnosis in a cystic fibrosis family: a combined molecular strategy for a precise diagnosis.
    Chávez-Saldaña M, García-Cavazos R, Vigueras RM, Orozco L.
    Rev Invest Clin; 2011 Mar; 63(4):433-5. PubMed ID: 22364044
    [Abstract] [Full Text] [Related]

  • 16. Molecular analysis of northwestern Mexican patients with cystic fibrosis: screening of 10 known mutations. Mutations in brief no. 185. Online.
    Flores-Martínez SE, Dean M, Saiki RK, Gallegos-Arreola MP, Morán-Moguel MC, Sánchez-Corona J.
    Hum Mutat; 1998 Mar; 12(3):217-8. PubMed ID: 10660336
    [Abstract] [Full Text] [Related]

  • 17. Cystic fibrosis in a southern Brazilian population: characteristics of 90% of the alleles.
    Faucz FR, Gimenez J, Ramos MD, Pereira-Ferrari L, Estivill X, Raskin S, Casals T, Culpi L.
    Clin Genet; 2007 Sep; 72(3):218-23. PubMed ID: 17718859
    [Abstract] [Full Text] [Related]

  • 18. Analysis of DNA probes for the prenatal diagnosis of cystic fibrosis.
    Dry PJ, Wake S, Robertson CF, Colley P, Sheffield LJ.
    Med J Aust; 1989 Aug 07; 151(3):131, 133-6. PubMed ID: 2569157
    [Abstract] [Full Text] [Related]

  • 19. Mutation analysis of CFTR gene in 70 Iranian cystic fibrosis patients.
    Alibakhshi R, Zamani M.
    Iran J Allergy Asthma Immunol; 2006 Mar 07; 5(1):3-8. PubMed ID: 17242497
    [Abstract] [Full Text] [Related]

  • 20. Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers.
    Morral N, Nunes V, Casals T, Chillón M, Giménez J, Bertranpetit J, Estivill X.
    Hum Mol Genet; 1993 Jul 07; 2(7):1015-22. PubMed ID: 7689896
    [Abstract] [Full Text] [Related]

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