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 *

167 related articles for article (PubMed ID: 1645913)

  • 21. Detection of the cystic fibrosis delta-F508 mutation at autopsy by site-directed mutagenesis.
    Salcedo M; Chávez M; Ridaura C; Moreno M; Lezana JL; Orozco L
    Am J Med Genet; 1993 May; 46(3):268-70. PubMed ID: 8488869
    [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. Part I. Frequency of the delta F508 mutation in South African families with cystic fibrosis.
    Denter M; Ramsay M; Jenkins T
    S Afr Med J; 1992 Jul; 82(1):7-10. PubMed ID: 1641732
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular screening of cystic fibrosis patients.
    Fellowes AP; Murphy JM; Wesley AW; Dawson KP; George PM
    N Z Med J; 1991 Oct; 104(921):415-6. PubMed ID: 1923090
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Neonatal screening for the cystic fibrosis main mutation delta F508 in Estonia.
    Klaassen T; Teder M; Viikmaa M; Metspalu A
    J Med Screen; 1998; 5(1):16-9. PubMed ID: 9575453
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. [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]  

  • 28. Method for rapid, single reaction, direct screening of the delta F508 cystic fibrosis microdeletion.
    Whetsell L; Shaefer F
    Biotechniques; 1992 May; 12(5):698, 701. PubMed ID: 1515137
    [No Abstract]   [Full Text] [Related]  

  • 29. [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]  

  • 30. The frequency of the delta F508 mutation in the cystic fibrosis genes of 71 unrelated South African cystic fibrosis patients.
    Herbert JS; Retief AE
    S Afr Med J; 1992 Jul; 82(1):13-5. PubMed ID: 1641711
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Allele frequencies of cystic fibrosis-linked markers and F508 deletion in affected Hungarian families.
    Endreffy E; Burg K; Gyurkovits K; Kálmán M; László A; Raskó I
    Acta Paediatr Hung; 1992; 32(2):101-13. PubMed ID: 1356379
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Fluorescence-based oligonucleotide ligation assay for analysis of cystic fibrosis transmembrane conductance regulator gene mutations.
    Eggerding FA; Iovannisci DM; Brinson E; Grossman P; Winn-Deen ES
    Hum Mutat; 1995; 5(2):153-65. PubMed ID: 7538376
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Direct diagnosis of predominant mutation delta F508 associated with the mucoviscidosis gene].
    Férec C; Guillermit H; Verlingue C; Parent P; Puissant H; Jehanne M; Saleun JP
    Arch Fr Pediatr; 1990; 47(7):507-10. PubMed ID: 2256790
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Frequency of delta-F508 mutation and XV2C/KM19 haplotypes in Cuban cystic fibrosis families.
    Collazo T; Magarino C; Chavez R; Suardiaz B; Gispert S; Gomez M; Rojo M; Heredero L
    Hum Hered; 1995; 45(1):55-7. PubMed ID: 7896301
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Molecular-genetic analysis of certain mutations of the "cystic fibrosis gene" in Moldavia. Characteristics of molecular markers and their linkage with various mutations].
    Gimbovskaia SD; Kalinin VN; Ivashchenko TE; Baranov VS
    Genetika; 1994 Dec; 30(12):1616-20. PubMed ID: 7534245
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Cystic fibrosis gene mutations and linked RFLPs in the Slovenian population.
    Ravnik-Glavac M; Gasparini P; Peterlin B; Strukelj M; Glavac D; Canki-Klain N; Pignatti PF; Komel R
    Ann Genet; 1992; 35(2):85-8. PubMed ID: 1355957
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Detection of more than 94% cystic fibrosis mutations in a sample of Belgian population and identification of four novel mutations.
    Mercier B; Lissens W; Audrézet MP; Bonduelle M; Liebaers I; Ferec C
    Hum Mutat; 1993; 2(1):16-20. PubMed ID: 8477260
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The deletion F508 is the major gene mutation in a representative Belgian cystic fibrosis population.
    Bonduelle M; Lissens W; Malfroot A; Dab I; Liebaers I
    Hum Genet; 1990 Sep; 85(4):395-6. PubMed ID: 2210742
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A frame-shift mutation in the cystic fibrosis gene.
    White MB; Amos J; Hsu JM; Gerrard B; Finn P; Dean M
    Nature; 1990 Apr; 344(6267):665-7. PubMed ID: 1691449
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.