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 *

138 related articles for article (PubMed ID: 7687737)

  • 1. The isolation of disease genes by positional cloning.
    Wainwright BJ
    Med J Aust; 1993 Aug; 159(3):170-4. PubMed ID: 7687737
    [No Abstract]   [Full Text] [Related]  

  • 2. Of needles and haystacks: finding human disease genes by positional cloning.
    Collins FS
    Clin Res; 1991 Dec; 39(4):615-23. PubMed ID: 1764889
    [No Abstract]   [Full Text] [Related]  

  • 3. The cystic fibrosis gene: isolation and significance.
    Collins FS; Riordan JR; Tsui LC
    Hosp Pract (Off Ed); 1990 Oct; 25(10):47-57. PubMed ID: 1698801
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identifying human disease genes by positional cloning.
    Collins FS
    Harvey Lect; 1990-1991; 86():149-64. PubMed ID: 2152136
    [No Abstract]   [Full Text] [Related]  

  • 5. Reverse genetics and cystic fibrosis.
    Iannuzzi MC; Collins FS
    Am J Respir Cell Mol Biol; 1990 Apr; 2(4):309-16. PubMed ID: 1691007
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetics of neurofibromatosis 1 in Japan: mutation rate and paternal age effect.
    Takano T; Kawashima T; Yamanouchi Y; Kitayama K; Baba T; Ueno K; Hamaguchi H
    Hum Genet; 1992 May; 89(3):281-6. PubMed ID: 1351032
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular analysis of cystic fibrosis in the Hungarian population.
    Nemeti M; Louie E; Papp Z; Johnson JP
    Hum Genet; 1991 Aug; 87(4):511-2. PubMed ID: 1715311
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The delta F508 mutation and RFLP-linked loci in Spanish cystic fibrosis families.
    Peral B; Hernández-Chico C; San Millán JL; Granell R; Molano J; Carrasco S; Tellería JJ; Devoto M; Moreno F
    Hum Genet; 1991 Aug; 87(4):516-7. PubMed ID: 1715312
    [No Abstract]   [Full Text] [Related]  

  • 9. A cystic fibrosis patient with delta F508, G542X and a deletion at the D7S8 locus.
    Wagner K; Greil I; Schneditz P; Pommer M; Rosenkranz W
    Hum Mutat; 1994; 3(3):327-9. PubMed ID: 7517267
    [No Abstract]   [Full Text] [Related]  

  • 10. Approaches to localizing disease genes as applied to cystic fibrosis.
    Dean M; Drumm ML; Stewart C; Gerrard B; Perry A; Hidaka N; Cole JL; Collins FS; Iannuzzi MC
    Nucleic Acids Res; 1990 Jan; 18(2):345-50. PubMed ID: 1970161
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A de novo cystic fibrosis mutation: CGA (Arg) to TGA (stop) at codon 851 of the CFTR gene.
    White MB; Leppert M; Nielsen D; Zielenski J; Gerrard B; Stewart C; Dean M
    Genomics; 1991 Nov; 11(3):778-9. PubMed ID: 1723056
    [No Abstract]   [Full Text] [Related]  

  • 12. Absence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus.
    Sharland M; Taylor R; Patton MA; Jeffery S
    J Med Genet; 1992 Mar; 29(3):188-90. PubMed ID: 1348095
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A rare DNA variant in exon 15 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
    Chillón M; Palacio A; Nunes V; Estivill X
    Hum Genet; 1992 Dec; 90(4):474. PubMed ID: 1282900
    [No Abstract]   [Full Text] [Related]  

  • 14. Diagnosis of neurofibromatosis type 1 using RFLPs tightly linked to gene.
    Vivarelli R; Bartalani G; Berardi A; Calistri L; Balestri P; Fois A
    Childs Nerv Syst; 1993 Jun; 9(3):147-9. PubMed ID: 8104099
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Utility of internal markers to improve the accuracy of cystic fibrosis genotype analysis.
    Raskin S; Phillips JA; Vnencak-Jones C; Dawson E; Kaplan G; McClure M
    Biotechniques; 1992 Sep; 13(3):372-4. PubMed ID: 1382468
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Patterns of polymorphism and linkage disequilibrium for cystic fibrosis.
    Estivill X; Scambler PJ; Wainwright BJ; Hawley K; Frederick P; Schwartz M; Baiget M; Kere J; Williamson R; Farrall M
    Genomics; 1987 Nov; 1(3):257-63. PubMed ID: 2895728
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The gene for congenital chloride diarrhea maps close to but is distinct from the gene for cystic fibrosis transmembrane conductance regulator.
    Kere J; Sistonen P; Holmberg C; de la Chapelle A
    Proc Natl Acad Sci U S A; 1993 Nov; 90(22):10686-9. PubMed ID: 7504277
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Molecular biological analysis of cystic fibrosis--a model example for the strategy of "reverse genetics"].
    Coutelle C; Grade K
    Padiatr Grenzgeb; 1992; 31(2):73-95. PubMed ID: 1284810
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Frequency of delta F508 mutation and haplotype analysis in Austrian cystic fibrosis families.
    Larsen J; Georghiou A; Kury FD; Götz M; Sanz K; Dobianer K; Spona J
    Hum Genet; 1992 Jun; 89(4):464-5. PubMed ID: 1377660
    [No Abstract]   [Full Text] [Related]  

  • 20. Prenatal diagnosis for cystic fibrosis using SSCP analysis.
    Desgeorges M; Boulot P; Kjellberg P; Lefort G; Rolland M; Demaille J; Claustres M
    Prenat Diagn; 1993 Feb; 13(2):147-8. PubMed ID: 7681978
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.