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Journal Abstract Search


93 related items for PubMed ID: 1808887

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

  • 2. Non-allelic genetic heterogeneity of autosomal dominant polycystic kidney disease?
    Nørby S, Sørensen AW, Boesen P.
    Prog Clin Biol Res; 1989; 305():83-8. PubMed ID: 2762358
    [No Abstract] [Full Text] [Related]

  • 3.
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  • 4. [Localization of the gene for the adult form of polycystic kidneys on the short arm of chromosome 16].
    Breuning MH, Reeders ST, Goor N, Hogewind BL, van Es LA, Pearson PL.
    Ned Tijdschr Geneeskd; 1986 Apr 12; 130(15):689-92. PubMed ID: 3703046
    [No Abstract] [Full Text] [Related]

  • 5.
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  • 6. Phenotypic correlates of autosomal recessive (infantile) polycystic disease of kidney and liver: criteria for classification and genetic counseling.
    Herrin JT.
    Prog Clin Biol Res; 1989 Apr 12; 305():45-54. PubMed ID: 2668974
    [No Abstract] [Full Text] [Related]

  • 7. Recent advances in the genetics of renal cystic disease.
    Reeders ST, Germino GG, Gillespie GA.
    Mol Biol Med; 1989 Feb 12; 6(1):81-6. PubMed ID: 2666822
    [No Abstract] [Full Text] [Related]

  • 8. A study of genetic linkage heterogeneity in adult polycystic kidney disease.
    Reeders ST, Breuning MH, Ryynanen MA, Wright AF, Davies KE, King AW, Watson ML, Weatherall DJ.
    Trans Assoc Am Physicians; 1986 Feb 12; 99():154-60. PubMed ID: 2885960
    [Abstract] [Full Text] [Related]

  • 9. [Autosomal dominant polycystic kidney disease. Early diagnosis using DNA marker analysis].
    Nørby S.
    Ugeskr Laeger; 1987 Sep 28; 149(40):2715-8. PubMed ID: 3451509
    [No Abstract] [Full Text] [Related]

  • 10. Glomerulocystic kidney diseases.
    Bernstein J, Landing BH.
    Prog Clin Biol Res; 1989 Sep 28; 305():27-43. PubMed ID: 2668973
    [No Abstract] [Full Text] [Related]

  • 11. [Autosomal dominant polycystic kidney and genetic markers of chromosome 16].
    Ferec C, Bourbigot B, Simon P, Whebe B, Treguer H, Hervé JP, Saleun JP, Cledes J.
    Nephrologie; 1990 Sep 28; 11(2):79-82. PubMed ID: 1975432
    [Abstract] [Full Text] [Related]

  • 12. [Indirect genotype analysis in 2 families with early manifestation of autosome dominant polycystic nephropathy].
    Schuster V, Uhlhaas S, Horwitz AE, Zerres K.
    Klin Padiatr; 1996 Sep 28; 208(3):110-3. PubMed ID: 8676597
    [Abstract] [Full Text] [Related]

  • 13. [Autosomal dominant hereditary polycystic kidney disease--the attitude of persons at risk to early diagnosis].
    Stephan M, Zerres K.
    Psychother Psychosom Med Psychol; 1988 Jul 28; 38(7):251-8. PubMed ID: 3212175
    [No Abstract] [Full Text] [Related]

  • 14. A gene (ETM) for essential tremor maps to chromosome 2p22-p25.
    Higgins JJ, Pho LT, Nee LE.
    Mov Disord; 1997 Nov 28; 12(6):859-64. PubMed ID: 9399207
    [Abstract] [Full Text] [Related]

  • 15. Liver cysts in patients with autosomal dominant polysystic kidney disease.
    Gandhi RM, Patil RA, Mehta NP, Thomas C.
    J Assoc Physicians India; 1993 Nov 28; 41(11):723. PubMed ID: 8005928
    [No Abstract] [Full Text] [Related]

  • 16. [Genetic defects underlying polycystic liver disease are discovered].
    Tahvanainen E, Tahvanainen P, Kääriäinen H, Höckerstedt K.
    Duodecim; 2004 Nov 28; 120(9):1081-4. PubMed ID: 15232849
    [No Abstract] [Full Text] [Related]

  • 17. [Cystic kidneys in children].
    Oemar BS, Hoyer PF, Ehrich JH, Offner G, Krohn HP, Brodehl J.
    Monatsschr Kinderheilkd; 1989 Jun 28; 137(6):314-20. PubMed ID: 2668742
    [Abstract] [Full Text] [Related]

  • 18. Explant culture of human polycystic kidney.
    McAteer JA, Carone FA, Grantham JJ, Kempson SA, Gardner KD, Evan AP.
    Lab Invest; 1988 Jul 28; 59(1):126-36. PubMed ID: 3392957
    [Abstract] [Full Text] [Related]

  • 19. [Current opinions about the etiology and pathogenesis of autosomal dominant polycystic kidney disease (ADPKD). I. Selected genetic aspects and mechanisms of cyst formation].
    Jasik P, Sułowicz W, Kraśniak A, Stompór T.
    Przegl Lek; 1998 Jul 28; 55(10):542-8. PubMed ID: 10224870
    [Abstract] [Full Text] [Related]

  • 20. Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.
    Hsia YE, Appadorai V, Breg WR, Howard RO.
    Birth Defects Orig Artic Ser; 1974 Jul 28; 10(8):19-25. PubMed ID: 4142400
    [No Abstract] [Full Text] [Related]


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