BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 2210747)

  • 21. The delta F508 mutation in cystic fibrosis patients of southern Italy.
    Sebastio G; Castiglione O; Incerti B; Salvatore D; Santamaria F
    Hum Genet; 1990 Sep; 85(4):430-1. PubMed ID: 2210764
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Frequency of the delta F508 mutation and flanking marker haplotypes at the CF locus from 167 Czech families.
    Macek M; Vavrová V; Böhm I; Stuhrmann M; Reis A; Duspivová R; Macek M; Sperling K; Krawczak M; Schmidtke J
    Hum Genet; 1990 Sep; 85(4):417-8. PubMed ID: 2210755
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene.
    Dörk T; Wulbrand U; Richter T; Neumann T; Wolfes H; Wulf B; Maass G; Tümmler B
    Hum Genet; 1991 Aug; 87(4):441-6. PubMed ID: 1715308
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Frequency of the F508 deletion in cystic fibrosis patients from the European part of the USSR.
    Baranov VS; Ivaschenko TE; Gorbunova VN; Livshitz LA; Venozinskis MT; Gembovskaya SA; Kalinin VN; Romanenko OP; Gembitzkaya TE; Orlov AV
    Hum Genet; 1991 May; 87(1):61-4. PubMed ID: 2037283
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF families.
    Novelli G; Gasparini P; Savoia A; Pignatti PF; Sangiuolo F; Dallapiccola B
    Hum Genet; 1990 Sep; 85(4):420-1. PubMed ID: 2210757
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular bases for cystic fibrosis in the Sardinian population.
    Leoni GB; Rosatelli C; Sardu R; Scarpa G; Silvetti M; Cao A
    Hum Genet; 1990 Sep; 85(4):415. PubMed ID: 2210754
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Frequency of the delta F508 and exon 11 mutations in Norwegian cystic fibrosis patients.
    Eiklid K; Tranebjaerg L; Eiken HG; Pedersen JC; Michalsen H; Fluge G; Schwartz M; Nilsen BR; Bolle R; Skyberg D
    Clin Genet; 1993 Jul; 44(1):12-4. PubMed ID: 7691448
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Cystic fibrosis mutation delta F508 in Finland: other mutations predominate.
    Kere J; Savilahti E; Norio R; Estivill X; de la Chapelle A
    Hum Genet; 1990 Sep; 85(4):413-5. PubMed ID: 2210753
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Cystic fibrosis haplotype association and the delta F508 mutation in adult British CF patients.
    Santis G; Osborne L; Knight R; Ramsay M; Williamson R; Hodson M
    Hum Genet; 1990 Sep; 85(4):424-5. PubMed ID: 2210760
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A dimorphic 4-bp repeat in the cystic fibrosis gene is in absolute linkage disequilibrium with the delta F508 mutation: implications for prenatal diagnosis and mutation origin.
    Chehab FF; Johnson J; Louie E; Goossens M; Kawasaki E; Erlich H
    Am J Hum Genet; 1991 Feb; 48(2):223-6. PubMed ID: 1990833
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Frequency of delta F508 and haplotype association in Austrian cystic fibrosis families.
    Wagner K; Zach M; Rosenkranz W
    Hum Genet; 1992 Jun; 89(4):437-8. PubMed ID: 1377659
    [TBL] [Abstract][Full Text] [Related]  

  • 32. First analysis of the F508 deletion in cystic fibrosis patients from the GDR.
    Grade K; Will K; Szibor R; Gedschold J; Brückner R; Bauer I; Giermann K; Gorki H; Hein J; Brell U
    Hum Genet; 1990 Sep; 85(4):406-7. PubMed ID: 1976592
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular diagnosis of cystic fibrosis in Maritime Canada.
    Corsten PG; Blight CE; Riddell DC; Hamilton DC; Cole DE
    Clin Invest Med; 1994 Feb; 17(1):1-8. PubMed ID: 7909728
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Distribution of the delta F508 mutation in 194 Spanish cystic fibrosis families.
    Chillón M; Nunes V; Casals T; Giménez FJ; Fernández E; Benítez J; Estivill X
    Hum Genet; 1990 Sep; 85(4):396-7. PubMed ID: 2210743
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Gradient of distribution in Europe of the major CF mutation and of its associated haplotype. European Working Group on CF Genetics (EWGCFG).
    Hum Genet; 1990 Sep; 85(4):436-45. PubMed ID: 2210767
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Association between haplotypes and specific mutations in Swiss cystic fibrosis families.
    Liechti-Gallati S; Malik N; Alkan M; Maechler M; Morris M; Thonney F; Sennhauser F; Moser H
    Pediatr Res; 1991 Oct; 30(4):304-8. PubMed ID: 1683481
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The prevalence of the deletion F508 in a Belgian cystic fibrosis population.
    Lissens W; Bonduelle M; Malfroot A; Dab I; Liebaers I
    Adv Exp Med Biol; 1991; 290():369-70. PubMed ID: 1950750
    [No Abstract]   [Full Text] [Related]  

  • 38. Cystic fibrosis mutations in North American populations of French ancestry: analysis of Quebec French-Canadian and Louisiana Acadian families.
    Rozen R; Schwartz RH; Hilman BC; Stanislovitis P; Horn GT; Klinger K; Daigneault J; De Braekeleer M; Kerem B; Tsui L
    Am J Hum Genet; 1990 Oct; 47(4):606-10. PubMed ID: 2220803
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Diagnostic value of the deletion of the delta F508 gene in cystic fibrosis].
    Fernández García E; Nunes Martínez V; Ibáñez Olias MA; Benítez Ortíz J
    An Esp Pediatr; 1991 Nov; 35(5):307-8. PubMed ID: 1785742
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genotyping of the Spanish cystic fibrosis population at the delta F508 mutation site and RFLP linked loci.
    Jaume-Roig B; Simon-Bouy B; Taillandier A; Serre JL; Antich J; Bellon J; Boué J; Boué A
    Hum Genet; 1990 Sep; 85(4):410-1. PubMed ID: 1976593
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.