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Journal Abstract Search

179 related items for PubMed ID: 10660962

  • 1. Improvement of preimplantation genetic diagnosis (PGD) for the cystic fibrosis mutation delta F508 by fluorescent polymerase chain reaction.
    Moutou C, Viville S.
    Prenat Diagn; 1999 Dec; 19(13):1248-50. PubMed ID: 10660962
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  • 4. Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders.
    Harper JC, Wells D, Piyamongkol W, Abou-Sleiman P, Apessos A, Ioulianos A, Davis M, Doshi A, Serhal P, Ranieri M, Rodeck C, Delhanty JD.
    Prenat Diagn; 2002 Jun; 22(6):525-33. PubMed ID: 12116320
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  • 5. Cystic fibrosis: frequency of delta f508 and g542x mutations in Cordoba, Argentina.
    Saleh MC, Botelli A, Melano de Botelli M, Rezzonico CA, Argaraña CE.
    Medicina (B Aires); 1996 Jun; 56(1):14-6. PubMed ID: 8734924
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  • 6. Approaches for cystic fibrosis diagnosis.
    Findlay I.
    Hum Reprod; 1997 Nov; 12(11 Suppl):166-9. PubMed ID: 9433974
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  • 9. [Correlation between phenotype and genotype in a group of patients with cystic fibrosis].
    Navarro H, Kolbach M, Repetto G, Guiraldes E, Harris P, Foradori A, Poggi H, Sánchez I.
    Rev Med Chil; 2002 May; 130(5):475-81. PubMed ID: 12143267
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  • 11. Optimal polymerase chain reaction amplification for preimplantation diagnosis in cystic fibrosis (delta F508).
    Cui KH, Haan EA, Wang LJ, Matthews CD.
    BMJ; 1995 Aug 26; 311(7004):536-40. PubMed ID: 7545043
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  • 12. [Frequency of delta F508 mutation in Venezuelan patients with cystic fibrosis].
    Morales-Machin A, Borjas-Fajardo L, Pineda L, González S, Delgado W, Zabala W, Fernández E.
    Invest Clin; 2004 Jun 26; 45(2):121-30. PubMed ID: 15211979
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  • 15. The cystic fibrosis delta F508 gene mutation and cancer.
    Padua RA, Warren N, Grimshaw D, Smith M, Lewis C, Whittaker J, Laidler P, Wright P, Douglas-Jones A, Fenaux P, Sharma A, Horgan K, West R.
    Hum Mutat; 1997 Jun 26; 10(1):45-8. PubMed ID: 9222759
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  • 18. [Preclinical study of preimplantation genetic diagnosis in animal].
    Ji Y, Zhao Y, Sheng Y.
    Zhonghua Fu Chan Ke Za Zhi; 2000 Aug 26; 35(8):462-4. PubMed ID: 11776197
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  • 20. A novel nonsense mutation, S466Xa in exon 10 of the cystic fibrosis transmembrane conductance regulator gene.
    Mittre H, Barre M, Leymarie P.
    Hum Mutat; 1996 Aug 26; 8(4):392-3. PubMed ID: 8956053
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