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Journal Abstract Search

138 related items for PubMed ID: 2311311

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis of cystic fibrosis by chorionic villus sampling using 12 polymorphic deoxyribonucleic acid markers.
    Nugent CE, Gravius T, Green P, Larsen JW, MacMillin MD, Donis-Keller H.
    Obstet Gynecol; 1988 Feb; 71(2):213-5. PubMed ID: 3422111
    [Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis of cystic fibrosis by using linked DNA markers in 138 pregnancies at 1-in-4 risk.
    Feldman GL, Lewiston N, Fernbach SD, O'Brien WE, Williamson R, Wainwright BJ, Beaudet AL.
    Am J Med Genet; 1989 Jun; 33(2):238-41. PubMed ID: 2569827
    [Abstract] [Full Text] [Related]

  • 4. 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 Jun; 1(3-4):211-7. PubMed ID: 1982988
    [Abstract] [Full Text] [Related]

  • 5. 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 07; 151(3):131, 133-6. PubMed ID: 2569157
    [Abstract] [Full Text] [Related]

  • 6. [Use of the recombinant DNA technic in studying cystic fibrosis in 14 Spanish families: detection of carriers and healthy subjects].
    Fernández García E, Benítez Ortiz J, Villamar López M, Ayuso García C, Ramos Corrales C, Sánchez Cascos A, Baiget M, Del Río E.
    An Esp Pediatr; 1989 Apr 07; 30(4):251-4. PubMed ID: 2568107
    [Abstract] [Full Text] [Related]

  • 7. Sweat chloride concentrations in infants homozygous or heterozygous for F508 cystic fibrosis.
    Farrell PM, Koscik RE.
    Pediatrics; 1996 Apr 07; 97(4):524-8. PubMed ID: 8632940
    [Abstract] [Full Text] [Related]

  • 8. First trimester diagnosis of cystic fibrosis with linked DNA probes.
    Németi M, Papp Z.
    Acta Univ Carol Med (Praha); 1990 Apr 07; 36(1-4):135-8. PubMed ID: 1983382
    [Abstract] [Full Text] [Related]

  • 9. [DNA diagnosis of monogene hereditary diseases exemplified by phenylketonuria and mucoviscidosis].
    Trefz FK, Lichter-Konecki U, Krawczak M, Schmidtke J, Dueck M, Nützenadel W, Konecki DS.
    Monatsschr Kinderheilkd; 1989 Apr 07; 137(4):201-7. PubMed ID: 2659975
    [Abstract] [Full Text] [Related]

  • 10. Borderline sweat test: Utility and limits of genetic analysis for the diagnosis of cystic fibrosis.
    Seia M, Costantino L, Paracchini V, Porcaro L, Capasso P, Coviello D, Corbetta C, Torresani E, Magazzù D, Consalvo V, Monti A, Costantini D, Colombo C.
    Clin Biochem; 2009 May 07; 42(7-8):611-6. PubMed ID: 19318035
    [Abstract] [Full Text] [Related]

  • 11. Polymorphic DNA markers linked to cystic fibrosis locus in 20 Italian nuclear families.
    Novelli G, Potenza L, Ruzzo A, Dallapiccola B.
    Gene Geogr; 1987 Dec 07; 1(3):193-9. PubMed ID: 3154126
    [Abstract] [Full Text] [Related]

  • 12. Pancreatic function and extended mutation analysis in DeltaF508 heterozygous infants with an elevated immunoreactive trypsinogen but normal sweat electrolyte levels.
    Massie RJ, Wilcken B, Van Asperen P, Dorney S, Gruca M, Wiley V, Gaskin K.
    J Pediatr; 2000 Aug 07; 137(2):214-20. PubMed ID: 10931414
    [Abstract] [Full Text] [Related]

  • 13. [DNA analysis and prenatal diagnosis in cystic fibrosis].
    Schnedl W, Weipoltshammer K.
    Wien Klin Wochenschr; 1991 Aug 07; 103(2):29-33. PubMed ID: 2024525
    [Abstract] [Full Text] [Related]

  • 14. Sweat electrolyte and cystic fibrosis mutation analysis allows early diagnosis in Brazilian children with clinical signs compatible with cystic fibrosis.
    Rabbi-Bortolini E, Bernardino AL, Lopes AL, Ferri AS, Passos-Bueno MR, Zatz M.
    Am J Med Genet; 1998 Apr 01; 76(4):288-90. PubMed ID: 9545091
    [Abstract] [Full Text] [Related]

  • 15. The application of molecular genetics to the study of the basic defect causing cystic fibrosis.
    Estivill X, Bates G, Bell G, Farrall M, Frederick P, Hawley K, Kruyer H, Lench N, Scrambler P, Stanier P.
    Prog Clin Biol Res; 1987 Apr 01; 254():181-90. PubMed ID: 2893385
    [Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of cystic fibrosis in a highly heterogeneous population.
    Casals T, Gimenez J, Ramos MD, Nunes V, Estivill X.
    Prenat Diagn; 1996 Mar 01; 16(3):215-22. PubMed ID: 8710774
    [Abstract] [Full Text] [Related]

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  • 19. [Haplotypes associated with the cystic fibrosis gene (CF)].
    Ferec C.
    J Genet Hum; 1988 Dec 01; 36(5):413-24. PubMed ID: 2905729
    [Abstract] [Full Text] [Related]

  • 20. Further data supporting linkage between cystic fibrosis and the met oncogene and haplotype analysis with met and pJ3.11.
    Farrall M, Watson E, Bates G, Bell G, Bell J, Davies KA, Estivill X, Kruyer H, Law HY, Lench N.
    Am J Hum Genet; 1986 Dec 01; 39(6):713-9. PubMed ID: 3467586
    [Abstract] [Full Text] [Related]

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