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 *

173 related articles for article (PubMed ID: 8198131)

  • 21. Cytogenetic and fluorescence in situ hybridization characterization of chromosome 1 rearrangements in head and neck carcinomas delineate a target region for deletions within 1p11-1p13.
    Jin Y; Jin C; Wennerberg J; Mertens F; Höglund M
    Cancer Res; 1998 Dec; 58(24):5859-65. PubMed ID: 9865746
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A new deletion of 18q23 with few typical features of the 18q- syndrome.
    Kohonen-Corish M; Strathdee G; Overhauser J; McDonald T; Jammu V
    J Med Genet; 1996 Mar; 33(3):240-3. PubMed ID: 8728701
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Preferential loss of the paternal alleles in the 18q- syndrome.
    Cody JD; Pierce JF; Brkanac Z; Plaetke R; Ghidoni PD; Kaye CI; Leach RJ
    Am J Med Genet; 1997 Mar; 69(3):280-6. PubMed ID: 9096757
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Global brain dysmyelination with above-average verbal skills in 18q- syndrome with a 17 Mb terminal deletion.
    Netzer C; Helmstaedter C; Ehrbrecht A; Engels H; Schwanitz G; Urbach H; Schröder R; Weber RG; Kornblum C
    Acta Neurol Scand; 2006 Aug; 114(2):133-8. PubMed ID: 16867037
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Development of diagnostic tools for the analysis of 5p deletions using interphase FISH.
    Gersh M; Grady D; Rojas K; Lovett M; Moyzis R; Overhauser J
    Cytogenet Cell Genet; 1997; 77(3-4):246-51. PubMed ID: 9284926
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Detection of a concomitant distal deletion in an inverted duplication of chromosome 3. Is there an overall mechanism for the origin of such duplications/deficiencies?
    Jenderny J; Poetsch M; Hoeltzenbein M; Friedrich U; Jauch A
    Eur J Hum Genet; 1998; 6(5):439-44. PubMed ID: 9801868
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The tricho-rhino-phalangeal syndromes: frequency and parental origin of 8q deletions.
    Nardmann J; Tranebjaerg L; Horsthemke B; Lüdecke HJ
    Hum Genet; 1997 May; 99(5):638-43. PubMed ID: 9150732
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Partial deletion of 18p and partial duplication of 18q caused by a paternal pericentric inversion.
    Israëls T; Hoovers J; Turpijn HM; Wijburg FA; Hennekam RC
    Clin Genet; 1996 Dec; 50(6):520-4. PubMed ID: 9147887
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.
    Horsley SW; Knight SJ; Nixon J; Huson S; Fitchett M; Boone RA; Hilton-Jones D; Flint J; Kearney L
    J Med Genet; 1998 Sep; 35(9):722-6. PubMed ID: 9733029
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Analysis of pericentromeric chromosome 21 specific YAC clones by FISH: identification of new markers for molecular-cytogenetic application.
    Yurov YB; Laurent AM; Marcais B; Vorsanova SG; Roizes G
    Hum Genet; 1995 Mar; 95(3):287-92. PubMed ID: 7868120
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Characterization of a t(10;12)(q24;p13) in a case of CML in transformation.
    Aguiar RC; Chase A; Oscier DG; Carapeti M; Goldman JM; Cross NC
    Genes Chromosomes Cancer; 1997 Dec; 20(4):408-11. PubMed ID: 9408758
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Congenital aural atresia in 18q deletion or de Grouchy syndrome.
    Nuijten I; Admiraal R; Van Buggenhout G; Cremers C; Frijns JP; Smeets D; van Ravenswaaij-Arts C
    Otol Neurotol; 2003 Nov; 24(6):900-6. PubMed ID: 14600472
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18.
    Boghosian-Sell L; Mewar R; Harrison W; Shapiro RM; Zackai EH; Carey J; Davis-Keppen L; Hudgins L; Overhauser J
    Am J Hum Genet; 1994 Sep; 55(3):476-83. PubMed ID: 8079991
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Fluorescence in situ hybridization evaluation of chromosome deletion patterns in prostate cancer.
    Huang SF; Xiao S; Renshaw AA; Loughlin KR; Hudson TJ; Fletcher JA
    Am J Pathol; 1996 Nov; 149(5):1565-73. PubMed ID: 8909246
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A 4-megabase YAC contig that spans the Langer-Giedion syndrome region on human chromosome 8q24.1: use in refining the location of the trichorhinophalangeal syndrome and multiple exostoses genes (TRPS1 and EXT1).
    Hou J; Parrish J; Lüdecke HJ; Sapru M; Wang Y; Chen W; Hill A; Siegel-Bartelt J; Northrup H; Elder FF
    Genomics; 1995 Sep; 29(1):87-97. PubMed ID: 8530105
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome.
    Ellison KA; Roth EJ; McCabe ER; Chinault AC; Zoghbi HY
    Am J Med Genet; 1993 Nov; 47(7):1124-34. PubMed ID: 8291533
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Anterior segment malformations in 18q- (de Grouchy) syndrome.
    Izquierdo NJ; Maumenee IH; Traboulsi EI
    Ophthalmic Paediatr Genet; 1993 Jun; 14(2):91-4. PubMed ID: 8233359
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Molecular analysis of three patients with interstitial deletions of chromosome band 14q31.
    Byth BC; Costa MT; Teshima IE; Wilson WG; Carter NP; Cox DW
    J Med Genet; 1995 Jul; 32(7):564-7. PubMed ID: 7562974
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10).
    Erdel M; Schuffenhauer S; Buchholz B; Barth-Witte U; Köchl S; Utermann B; Duba HC; Utermann G
    Hum Genet; 1996 Jun; 97(6):784-93. PubMed ID: 8641697
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Monosomy 18q syndrome and atypical Rett syndrome in a girl with an interstitial deletion (18)(q21.1q22.3).
    Gustavsson P; Kimber E; Wahlström J; Annerén G
    Am J Med Genet; 1999 Feb; 82(4):348-51. PubMed ID: 10051171
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.