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 *

98 related articles for article (PubMed ID: 8314565)

  • 1. Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13.
    Kooy RF; Van der Veen AY; Verlind E; Houwen RH; Scheffer H; Buys CH
    Hum Genet; 1993 Jun; 91(5):504-6. PubMed ID: 8314565
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A deletion hybrid breakpoint map of the chromosomal region 13q14-q21 orders 19 genetic markers in 10 intervals.
    Kooy RF; Verlind E; Houwen RH; Shapiro DN; Hawthorn LA; Cowell JK; Scheffer H; Buys CH
    Eur J Hum Genet; 1994; 2(1):59-65. PubMed ID: 7913868
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Isolation of new probes in the region of the Wilson disease locus, 13q14.2-->q14.3.
    Bull PC; Barwell JA; Hannah HT; Pautler SE; Higgins MJ; Lalande M; Cox DW
    Cytogenet Cell Genet; 1993; 64(1):12-7. PubMed ID: 8508673
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A 4.5-megabase yeast artificial chromosome contig from human chromosome 13q14.3 ordering 9 polymorphic microsatellites (22 sequence-tagged sites) tightly linked to the Wilson disease locus.
    White A; Tomfohrde J; Stewart E; Barnes R; Le Paslier D; Weissenbach J; Cavalli-Sforza L; Farrer L; Bowcock A
    Proc Natl Acad Sci U S A; 1993 Nov; 90(21):10105-9. PubMed ID: 8234264
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Long range restriction mapping of 13q14.3 focused on the Wilson disease region.
    Bull PC; Cox DW
    Genomics; 1993 Jun; 16(3):593-8. PubMed ID: 8325631
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of crossovers in Wilson disease families as reference points for a genetic localization of the gene.
    Scheffer H; Houwen RH; Te Meerman GJ; Loessner J; Bachmann B; Kunert E; Verlind E; Buys CH
    Hum Genet; 1992 Aug; 89(6):607-11. PubMed ID: 1511977
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Allelic association and linkage studies in Wilson disease.
    Thomas GR; Roberts EA; Rosales TO; Moroz SP; Lambert MA; Wong LT; Cox DW
    Hum Mol Genet; 1993 Sep; 2(9):1401-5. PubMed ID: 7902160
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Polymorphic microsatellites and Wilson disease (WD).
    Stewart EA; White A; Tomfohrde J; Osborne-Lawrence S; Prestridge L; Bonne-Tamir B; Scheinberg IH; St George-Hyslop P; Giagheddu M; Kim JW
    Am J Hum Genet; 1993 Oct; 53(4):864-73. PubMed ID: 8213814
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Occurrence of holoprosencephaly in chromosome 13 disorders cannot be explained by duplication/deficiency of a single locus.
    Wilson GN; Dasouki M; Barr M
    Am J Med Genet Suppl; 1986; 2():65-72. PubMed ID: 3146301
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The consistent 13q14 translocation breakpoint seen in chronic B-cell leukaemia (BCLL) involves deletion of the D13S25 locus which lies distal to the retinoblastoma predisposition gene.
    Hawthorn LA; Chapman R; Oscier D; Cowell JK
    Oncogene; 1993 Jun; 8(6):1415-9. PubMed ID: 8502470
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Eight closely linked loci place the Wilson disease locus within 13q14-q21.
    Bowcock AM; Farrer LA; Hebert JM; Agger M; Sternlieb I; Scheinberg IH; Buys CH; Scheffer H; Frydman M; Chajek-Saul T
    Am J Hum Genet; 1988 Nov; 43(5):664-74. PubMed ID: 3189332
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Isolation and regional localization of 25 anonymous DNA probes on a chromosome 13 hybrid panel.
    Houwen RH; Pautler SE; Barwell JA; Arden K; Buchanan JA; James CD; Cavenee WK; Buys CH; Cowell JK; Cox DW
    Cytogenet Cell Genet; 1991; 57(2-3):87-90. PubMed ID: 1914527
    [TBL] [Abstract][Full Text] [Related]  

  • 13. DNA markers for the diagnosis of Wilson disease.
    Houwen RH; Roberts EA; Thomas GR; Cox DW
    J Hepatol; 1993 Mar; 17(3):269-76. PubMed ID: 8100247
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson disease.
    Scheffer H; Kema IP; Kondo I; van der Veen AY; Ikeuchi T; Buys CH
    Hum Genet; 1987 Dec; 77(4):335-7. PubMed ID: 2891602
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The gene responsible for LEC hepatitis, located on rat chromosome 16, is the homolog to the human Wilson disease gene.
    Sasaki N; Hayashizaki Y; Muramatsu M; Matsuda Y; Ando Y; Kuramoto T; Serikawa T; Azuma T; Naito A; Agui T
    Biochem Biophys Res Commun; 1994 Jul; 202(1):512-8. PubMed ID: 8037756
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Close linkage of the Wilson's disease locus to D13S12 in the chromosomal region 13q21 and not to ESD in 13q14.
    Houwen RH; Scheffer H; te Meerman GJ; van der Vlies P; Buys CH
    Hum Genet; 1990 Oct; 85(5):560-2. PubMed ID: 2227943
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Cloning the Wilson disease gene].
    Riedel HD; Fitscher BA; Hefter H; Strohmeyer G; Stremmel W
    Z Gastroenterol; 1994 Aug; 32(8):472-3. PubMed ID: 7975792
    [No Abstract]   [Full Text] [Related]  

  • 18. Maternal origin of extra marker chromosome 1Q31.1-qter and 13pter-q12.12 in a child with dysmorhic features.
    Rao VB; Kerketta L; Korgaonkar S; Ghosh K; Mohanty D
    Genet Couns; 2005; 16(2):139-43. PubMed ID: 16082769
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A 13-year-old boy with cognitive impairment, retinoblastoma, and Wilson disease.
    Riley D; Wiznitzer M; Schwartz S; Zinn AB
    Neurology; 2001 Jul; 57(1):141-3. PubMed ID: 11445646
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterisation of molecular DNA rearrangements within the Xq12-q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA).
    Thomas NS; Chelly J; Zonana J; Davies KJ; Morgan S; Gault J; Rack KA; Buckle VJ; Brockdorff N; Clarke A
    Hum Mol Genet; 1993 Oct; 2(10):1679-85. PubMed ID: 8268921
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.