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211 related items for PubMed ID: 22364044

  • 1. 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; 63(4):433-5. PubMed ID: 22364044
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  • 5. [Non-invasive prenatal diagnosis of cystic fibrosis].
    Paterlini Bréchot P, Mouawia H, Saker A.
    Arch Pediatr; 2011 Jan; 18(1):111-8. PubMed ID: 21177083
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  • 7. Segregation analysis in cystic fibrosis at-risk family demonstrates that the M348K CFTR mutation is a rare innocuous polymorphism.
    D'Apice MR, Gambardella S, Russo S, Lucidi V, Nardone AM, Pietropolli A, Novelli G.
    Prenat Diagn; 2004 Dec 15; 24(12):981-3. PubMed ID: 15614862
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  • 11. XV-2c/KM-19 haplotype analysis of cystic fibrosis mutations in Mexican patients.
    Orozco L, González L, Chávez M, Velázquez R, Lezana JL, Saldaña Y, Villarreal T, Carnevale A.
    Am J Med Genet; 2001 Aug 15; 102(3):277-81. PubMed ID: 11484207
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  • 12. [Characterization of 3 microsatellites of the cystic fibrosis gene in Argentine families].
    Visich AA, Barreiro CZ, Chertkoff LP.
    Medicina (B Aires); 2001 Aug 15; 61(1):23-7. PubMed ID: 11265619
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  • 14. 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
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  • 15. New strategy for the prenatal detection/exclusion of paternal cystic fibrosis mutations in maternal plasma.
    Bustamante-Aragones A, Gallego-Merlo J, Trujillo-Tiebas MJ, de Alba MR, Gonzalez-Gonzalez C, Glover G, Diego-Alvarez D, Ayuso C, Ramos C.
    J Cyst Fibros; 2008 Nov 07; 7(6):505-10. PubMed ID: 18573697
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  • 16. Diagnostic usefulness of the polymorphism of the GT dinucleotide and the polythymidine tract in intron 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
    Cazeneuve C, Beldjord C, Kaplan JC, Bienvenu T.
    Ann Genet; 1995 Nov 07; 38(4):202-5. PubMed ID: 8629807
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  • 18. [Indirect cystic fibrosis carrier detection in two Chilean families by analysis of DNA polymorphisms closely linked to the CFTR gene].
    Riveros K N, Ríos H J.
    Rev Med Chil; 2005 Jun 07; 133(6):648-54. PubMed ID: 16075128
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  • 19. An update on cystic fibrosis screening.
    Goetzinger KR, Cahill AG.
    Clin Lab Med; 2010 Sep 07; 30(3):533-43. PubMed ID: 20638569
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  • 20. 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 Sep 07; 12(3):217-8. PubMed ID: 10660336
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