These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

109 related articles for article (PubMed ID: 8475954)

  • 21. Cystic fibrosis in Spain: high frequency of mutation G542X in the Mediterranean coastal area.
    Casals T; Nunes V; Palacio A; Giménez J; Gaona A; Ibáñez N; Morral N; Estivill X
    Hum Genet; 1993 Mar; 91(1):66-70. PubMed ID: 8454290
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genotype/phenotype association in cystic fibrosis: analyses of the delta F508, R553X, and 3905insT mutations.
    Liechti-Gallati S; Bonsall I; Malik N; Schneider V; Kraemer LG; Ruedeberg A; Moser H; Kraemer R
    Pediatr Res; 1992 Aug; 32(2):175-8. PubMed ID: 1380689
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cystic fibrosis mutations delta F508 and G542X in Jewish patients.
    Lerer I; Sagi M; Cutting GR; Abeliovich D
    J Med Genet; 1992 Feb; 29(2):131-3. PubMed ID: 1377276
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A single-tube multiplex system for the simultaneous detection of 10 common cystic fibrosis mutations.
    Axton RA; Brock DJ
    Hum Mutat; 1995; 5(3):260-2. PubMed ID: 7599637
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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; 56(1):14-6. PubMed ID: 8734924
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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; 2(7):1015-22. PubMed ID: 7689896
    [TBL] [Abstract][Full Text] [Related]  

  • 27. CFTR gene: molecular analysis in patients from South Brazil.
    Streit C; Burlamaque-Neto AC; de Abreu e Silva F; Giugliani R; Saraiva Pereira ML
    Mol Genet Metab; 2003 Apr; 78(4):259-64. PubMed ID: 12706377
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene.
    Reiss J; Cooper DN; Bal J; Slomski R; Cutting GR; Krawczak M
    Hum Genet; 1991 Aug; 87(4):457-61. PubMed ID: 1715309
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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; 98(3):336-44. PubMed ID: 8707306
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Spectrum of CFTR mutations in Argentine cystic fibrosis patients.
    Chertkoff L; Visich A; Bienvenu T; Grenoville M; Segal E; Carniglia L; Kaplan JC; Barreiro C
    Clin Genet; 1997 Jan; 51(1):43-7. PubMed ID: 9084934
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Analysis of five mutations of cystic fibrosis occurring in the Hungarian population].
    Németh K; Holics K; Ujhelyi R; Váradi A; Fekete G
    Orv Hetil; 1996 Apr; 137(17):899-903. PubMed ID: 8649752
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis.
    Sereth H; Shoshani T; Bashan N; Kerem BS
    Hum Genet; 1993 Oct; 92(3):289-95. PubMed ID: 7691712
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Application of multiplex ARMS and SSCP/HD analysis in molecular diagnosis of cystic fibrosis in Indian patients.
    Ashavaid TF; Kondkar AA; Dherai AJ; Raghavan R; Udani SV; Udwadia ZF; Desai D
    Mol Diagn; 2005; 9(2):59-66. PubMed ID: 16137181
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Frequency of the delta F508 deletion and G551D, R553X and G542X mutations in Yugoslav CF patients.
    Dabović BB; Radojković D; Minić P; Savić J; Savić A
    Hum Genet; 1992 Mar; 88(6):699-700. PubMed ID: 1551678
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification of three novel mutations in the CFTR gene using temperature-optimized non-radioactive conditions for SSCP analysis.
    Grade K; Grunewald I; Graupner I; Behrens F; Coutelle C
    Hum Genet; 1994 Aug; 94(2):154-8. PubMed ID: 7519167
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Molecular genetic analysis of TUB18 and TUB20 intragenic polymorphism and various mutations of the CFTR gene in the Moscow region].
    Sazonova MA; Amosenko FA; Kapranov NI; Kalinin VN
    Genetika; 1997 Sep; 33(9):1303-7. PubMed ID: 9445824
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Identification of common cystic fibrosis mutations in African-Americans with cystic fibrosis increases the detection rate to 75%.
    Macek M; Mackova A; Hamosh A; Hilman BC; Selden RF; Lucotte G; Friedman KJ; Knowles MR; Rosenstein BJ; Cutting GR
    Am J Hum Genet; 1997 May; 60(5):1122-7. PubMed ID: 9150159
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prevalence of cystic fibrosis mutations in the East German population.
    Coutelle C; Brückner R; Grade K; Behrens F; Gedschold J; Hein J; Szibor R; Bauer I; Brock J; Graupner I
    Hum Mutat; 1992; 1(2):109-12. PubMed ID: 1301197
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Screening for cystic fibrosis gene mutations by multiplex DNA amplification.
    Picci L; Anglani F; Scarpa M; Zacchello F
    Hum Genet; 1992 Mar; 88(5):552-6. PubMed ID: 1551658
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.