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Journal Abstract Search

527 related items for PubMed ID: 8710774

  • 21. Birth of a normal girl after in vitro fertilization and preimplantation diagnostic testing for cystic fibrosis.
    Handyside AH, Lesko JG, Tarín JJ, Winston RM, Hughes MR.
    N Engl J Med; 1992 Sep 24; 327(13):905-9. PubMed ID: 1381054
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  • 22. Analysis of the CFTR gene in the Spanish population: SSCP-screening for 60 known mutations and identification of four new mutations (Q30X, A120T, 1812-1 G-->A, and 3667del4).
    Chillón M, Casals T, Giménez J, Nunes V, Estivill X.
    Hum Mutat; 1994 Sep 24; 3(3):223-30. PubMed ID: 7517264
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  • 23. CFTR haplotypic variability for normal and mutant genes in cystic fibrosis families from southern France.
    Claustres M, Desgeorges M, Moine P, Morral N, Estivill X.
    Hum Genet; 1996 Sep 24; 98(3):336-44. PubMed ID: 8707306
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  • 24. Genetic characterisation of circulating fetal cells allows non-invasive prenatal diagnosis of cystic fibrosis.
    Saker A, Benachi A, Bonnefont JP, Munnich A, Dumez Y, Lacour B, Paterlini-Brechot P.
    Prenat Diagn; 2006 Oct 24; 26(10):906-16. PubMed ID: 16832834
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  • 25. Molecular genetic studies in monogenic and polygenic human diseases.
    Endreffy E, László, Szabó A, Román F, Kürti K, Kálmán M, Raskó I.
    Acta Biol Hung; 1997 Oct 24; 48(1):121-8. PubMed ID: 9199707
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  • 26. Distribution of 9 common mutations in the CFTR gene in Slovak cystic fibrosis patients.
    Kádasi L, Poláková H, Zatková A, Kayserová H.
    Gene Geogr; 1997 Apr 24; 11(1):51-6. PubMed ID: 9615214
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  • 27. [Clinical application of analysis of microsatellite markers in the prenatal diagnosis of cystic fibrosis].
    Ferenczi A, Homolya V, Szakács G, Németh K, Kiss E, Váradi A, Fekete G.
    Orv Hetil; 1997 Jan 26; 138(4):209-13. PubMed ID: 9072754
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  • 33. [Possibilities and prospects of the use of DNA analysis in the diagnosis and prevention of inherited disease in the Ukraine].
    Livshyts' LA, Gryshko VI, Kravchenko SA.
    Tsitol Genet; 1992 Jan 26; 26(4):35-42. PubMed ID: 1279869
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  • 36. [Molecular basis of phenotype heterogeneity in cystic fibrosis].
    Bienvenu T.
    Ann Biol Clin (Paris); 1997 Jan 26; 55(2):113-21. PubMed ID: 9180964
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  • 37. [Cystic fibrosis: the CFTR gene, its mutations, the genetic counseling].
    Goossens M, Ghanem N, Girodon E, Costes B, Fanen P.
    Rev Pneumol Clin; 1995 Jan 26; 51(3):130-6. PubMed ID: 7569574
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  • 38. [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 26; 130(5):475-81. PubMed ID: 12143267
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