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 *

260 related articles for article (PubMed ID: 2296270)

  • 1. Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosis.
    Lemna WK; Feldman GL; Kerem B; Fernbach SD; Zevkovich EP; O'Brien WE; Riordan JR; Collins FS; Tsui LC; Beaudet AL
    N Engl J Med; 1990 Feb; 322(5):291-6. PubMed ID: 2296270
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 327(13):905-9. PubMed ID: 1381054
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. New strategy for the prenatal detection/exclusion of paternal cystic fibrosis mutations in maternal plasma.
    Bustamante-Aragones A; Gallego-Merlo J; Trujillo-Tiebas MJ; de Alba MR; Gonzalez-Gonzalez C; Glover G; Diego-Alvarez D; Ayuso C; Ramos C
    J Cyst Fibros; 2008 Nov; 7(6):505-10. PubMed ID: 18573697
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis of cystic fibrosis in a highly heterogeneous population.
    Casals T; Gimenez J; Ramos MD; Nunes V; Estivill X
    Prenat Diagn; 1996 Mar; 16(3):215-22. PubMed ID: 8710774
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of DNA probes for the prenatal diagnosis of cystic fibrosis.
    Dry PJ; Wake S; Robertson CF; Colley P; Sheffield LJ
    Med J Aust; 1989 Aug; 151(3):131, 133-6. PubMed ID: 2569157
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Experience of an academic reference laboratory using automation for analysis of cystic fibrosis mutations.
    DeMarchi JM; Beaudet AL; Caskey CT; Richards CS
    Arch Pathol Lab Med; 1994 Jan; 118(1):26-32. PubMed ID: 8285831
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Mutation analysis and haplotype correlation for 139 cystic fibrosis patients from the Nebraska Regional Cystic Fibrosis Center.
    Traystman MD; Schulte N; Colombo JL; Sammut PH; Reilly P; Patel C; Acquazzino D; Simanek B; Anderson R; Kimberling WJ
    Hum Mutat; 1993; 2(1):7-15. PubMed ID: 7682884
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of cystic fibrosis.
    Kampmann W; Mathy L; Grzeschik KH; Driesel Aj; Bartholomé K; Neugebauer M; Olek K
    J Clin Chem Clin Biochem; 1989 Mar; 27(3):117-22. PubMed ID: 2651551
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [DNA analysis and prenatal diagnosis in cystic fibrosis].
    Schnedl W; Weipoltshammer K
    Wien Klin Wochenschr; 1991; 103(2):29-33. PubMed ID: 2024525
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat chloride concentrations.
    Highsmith WE; Burch LH; Zhou Z; Olsen JC; Boat TE; Spock A; Gorvoy JD; Quittel L; Friedman KJ; Silverman LM
    N Engl J Med; 1994 Oct; 331(15):974-80. PubMed ID: 7521937
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Prenatal molecular diagnosis of cystic fibrosis. Report of 3 cases].
    Morales-Machín A; Borjas-Fajardo L; Pineda-Del Villar L; Prieto-Carrasquero M; González S; Gutiérrez M; Delgado-Luengo W; Alvarez F; Barrera-Saldaña H
    Invest Clin; 1997 Sep; 38(3):145-53. PubMed ID: 9376420
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Identification of carriers by screening for delta F508 deletion in a multi-generation cystic fibrosis family.
    Claustres M; Desgeorges M; Kjellberg P; Demaille J
    Genet Couns; 1990; 1(3-4):211-7. PubMed ID: 1982988
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Prenatal diagnosis of cystic fibrosis by mutational analysis].
    Németi M; Papp C; Tóth-Pál E; Papp Z
    Orv Hetil; 1992 Jun; 133(23):1433-5. PubMed ID: 1603587
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Direct gene diagnosis of cystic fibrosis by allele-specific polymerase chain reactions.
    Wagner M; Schloesser M; Reiss J
    Mol Biol Med; 1990 Aug; 7(4):359-64. PubMed ID: 1978221
    [TBL] [Abstract][Full Text] [Related]  

  • 18. DNA analysis of cystic fibrosis in Brazil by direct PCR amplification from Guthrie cards.
    Raskin S; Phillips JA; Krishnamani MR; Vnencak-Jones C; Parker RA; Rozov T; Cardieri JM; Marostica P; Abreu F; Giugliani R
    Am J Med Genet; 1993 Jul; 46(6):665-9. PubMed ID: 8362909
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Prenatal diagnosis of cystic fibrosis in Tunisia. Apropos of the deltaF508 mutation].
    Messaoud T; Abdennebi M; Ben Ammar B; Fattoum S
    Tunis Med; 1995 Jan; 73(1):43-6. PubMed ID: 9506121
    [No Abstract]   [Full Text] [Related]  

  • 20. A 31-mutation assay for cystic fibrosis testing in the clinical molecular diagnostics laboratory.
    Wall J; Cai S; Chehab FF
    Hum Mutat; 1995; 5(4):333-8. PubMed ID: 7627189
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.