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123 related items for PubMed ID: 1296525

  • 1. Trisomy 21 mosaicism in two subjects from two generations.
    Casati A, Giorgi R, Lanza A, Raimondi E, Vagnarelli P, Mondello C, Ghetti P, Piazzi G, Nuzzo F.
    Ann Genet; 1992; 35(4):245-50. PubMed ID: 1296525
    [Abstract] [Full Text] [Related]

  • 2. Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.
    Crowe CA, Schwartz S, Black CJ, Jaswaney V.
    Am J Med Genet; 1997 Sep 05; 71(4):406-13. PubMed ID: 9286446
    [Abstract] [Full Text] [Related]

  • 3. Chromosome missegregation and trisomy 21 mosaicism in Alzheimer's disease.
    Geller LN, Potter H.
    Neurobiol Dis; 1999 Jun 05; 6(3):167-79. PubMed ID: 10408806
    [Abstract] [Full Text] [Related]

  • 4. Centromeric DNA break in a 10;16 reciprocal translocation associated with trisomy 16 confined placental mosaicism and maternal uniparental disomy for chromosome 16.
    Wang JC, Mamunes P, Kou SY, Schmidt J, Mao R, Hsu WT.
    Am J Med Genet; 1998 Dec 04; 80(4):418-22. PubMed ID: 9856575
    [Abstract] [Full Text] [Related]

  • 5. [Cytogenetic study of 121 patients suffering from various hematologic neoplasms using the in situ hybridization technique].
    Pérez Losada A, Solé F, Woessner S, Florensa L, Besses C, Espinet B, Caballín MR, García Eroles L, Sans-Sabrafén J.
    Sangre (Barc); 1996 Jun 04; 41(3):201-9. PubMed ID: 8755208
    [Abstract] [Full Text] [Related]

  • 6. Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues.
    Micale MA, Wolff DJ, Dickerman LH, Redline R, Conroy JM, Schwartz S.
    Prenat Diagn; 1996 Oct 04; 16(10):893-7. PubMed ID: 8938057
    [Abstract] [Full Text] [Related]

  • 7. Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies.
    Kulharya AS, Lovell CM, Flannery DB.
    Am J Med Genet; 2002 Dec 15; 113(4):367-70. PubMed ID: 12457409
    [Abstract] [Full Text] [Related]

  • 8. Examination of trisomy 13, 18 and 21 foetal tissues at different gestational ages using FISH.
    Moore GE, Ruangvutilert P, Chatzimeletiou K, Bell G, Chen CK, Johnson P, Harper JC.
    Eur J Hum Genet; 2000 Mar 15; 8(3):223-8. PubMed ID: 10780789
    [Abstract] [Full Text] [Related]

  • 9. Confined placental mosaicism for trisomies 2, 3, 7, 8, 9, 16, and 22: their incidence, likely origins, and mechanisms for cell lineage compartmentalization.
    Wolstenholme J.
    Prenat Diagn; 1996 Jun 15; 16(6):511-24. PubMed ID: 8809892
    [Abstract] [Full Text] [Related]

  • 10. Comparative analysis of the rates of chromosome damage induced by bleomycin radiomimetic in human trisomic and diploid lymphocytes: in vitro cultures from a mosaic of a Down's syndrome individual.
    Cano J, Caparros MM, Pretel A.
    Cytobios; 1995 Jun 15; 83(334):159-66. PubMed ID: 8620688
    [Abstract] [Full Text] [Related]

  • 11. Atypical Down syndrome phenotype in a girl with 21;21 translocation trisomy.
    Tuysuz B, Yavuz A, Ozdil M, Caferler J, Ozon H.
    Genet Couns; 2010 Jun 15; 21(1):61-7. PubMed ID: 20420031
    [Abstract] [Full Text] [Related]

  • 12. Trisomy 15 mosaic derived from trisomic conceptus: report of a case and a review.
    Markovic VD, Chitayat DA, Ritchie SM, Chodakowski BA, Hutton EM.
    Am J Med Genet; 1996 Feb 02; 61(4):363-70. PubMed ID: 8834049
    [Abstract] [Full Text] [Related]

  • 13. Trisomy 15 CPM: probable origins, pregnancy outcome and risk of fetal UPD: European Collaborative Research on Mosaicism in CVS (EUCROMIC).
    Prenat Diagn; 1999 Jan 02; 19(1):29-35. PubMed ID: 10073903
    [Abstract] [Full Text] [Related]

  • 14. Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies.
    Genuardi M, Tozzi C, Pomponi MG, Stagni ML, Della Monica M, Scarano G, Calvieri F, Torrisi L, Neri G.
    Eur J Hum Genet; 1999 Jan 02; 7(4):421-6. PubMed ID: 10352932
    [Abstract] [Full Text] [Related]

  • 15. Failure of PHA-stimulated i(12p) lymphocytes to divide in Pallister-Killian syndrome.
    Reeser SL, Wenger SL.
    Am J Med Genet; 1992 Apr 01; 42(6):815-9. PubMed ID: 1554020
    [Abstract] [Full Text] [Related]

  • 16. Histopathology and molecular cytogenetics of a corneal opacity associated with the trisomy 8 mosaic syndrome (46,XY/47,XY, +8).
    Scott JA, Howard PJ, Smith PA, Fryer A, Easty DL, Patterson A, Kaye SB.
    Cornea; 1997 Jan 01; 16(1):35-41. PubMed ID: 8985632
    [Abstract] [Full Text] [Related]

  • 17. Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicism.
    Kosaki R, Hanai S, Kakishima H, Okada MA, Hayashi S, Ito Y, Takahashi T, Kosaki K, Okuyama T.
    Congenit Anom (Kyoto); 2006 Jun 01; 46(2):115-7. PubMed ID: 16732770
    [Abstract] [Full Text] [Related]

  • 18. Age-associated chromosome 21 loss in Down syndrome: possible relevance to mosaicism and Alzheimer disease.
    Percy ME, Markovic VD, Dalton AJ, McLachlan DR, Berg JM, Rusk AC, Somerville MJ, Chodakowski B, Andrews DF.
    Am J Med Genet; 1993 Mar 01; 45(5):584-8. PubMed ID: 8456829
    [Abstract] [Full Text] [Related]

  • 19. Trisomy 7 CVS mosaicism: pregnancy outcome, placental and DNA analysis in 14 cases.
    Kalousek DK, Langlois S, Robinson WP, Telenius A, Bernard L, Barrett IJ, Howard-Peebles PN, Wilson RD.
    Am J Med Genet; 1996 Nov 11; 65(4):348-52. PubMed ID: 8923948
    [Abstract] [Full Text] [Related]

  • 20. Numerical abnormalities of chromosome 7 in human prostate cancer detected by fluorescence in situ hybridization (FISH) on paraffin-embedded tissue sections with centromere-specific DNA probes.
    Zitzelsberger H, Szücs S, Weier HU, Lehmann L, Braselmann H, Enders S, Schilling A, Breul J, Höfler H, Bauchinger M.
    J Pathol; 1994 Apr 11; 172(4):325-35. PubMed ID: 8207613
    [Abstract] [Full Text] [Related]

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