BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

86 related articles for article (PubMed ID: 8020975)

  • 1. Linkage mapping of the gene for type III collagen (COL3A1) to human chromosome 2q using a VNTR polymorphism.
    Tiller GE; Polumbo PA; Summar ML
    Genomics; 1994 Mar; 20(2):275-7. PubMed ID: 8020975
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Regional mapping of loci from human chromosome 2q to sheep chromosome 2q.
    Ansari HA; Pearce PD; Maher DW; Malcolm AA; Wood NJ; Phua SH; Broad TE
    Genomics; 1994 Mar; 20(1):122-4. PubMed ID: 8020939
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Physical mapping by PFGE localizes the COL3A1 and COL5A2 genes to a 35-kb region on human chromosome 2.
    Cutting GR; McGinniss MJ; Kasch LM; Tsipouras P; Antonarakis SE
    Genomics; 1990 Oct; 8(2):407-10. PubMed ID: 1979060
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Single-strand conformation polymorphism (SSCP) analysis of the COL3A1 gene detects a mutation that results in the substitution of glycine 1009 to valine and causes severe Ehlers-Danlos syndrome type IV.
    Nuytinck L; De Paepe A; Renard JP; Adriaens F; Leroy J
    Hum Mutat; 1994; 3(3):268-74. PubMed ID: 8019562
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dinucleotide repeat loci contribute highly informative genetic markers to the human chromosome 2 linkage map.
    Todd S; Sherman SL; Naylor SL
    Genomics; 1993 Jun; 16(3):612-8. PubMed ID: 8100800
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fluorescence in situ hybridization mapping of 25 markers on distal human chromosome 2q surrounding the human Waardenburg syndrome, type I (WS1) locus (PAX3 gene).
    Lu-Kuo J; Ward DC; Spritz RA
    Genomics; 1993 Apr; 16(1):173-9. PubMed ID: 8486353
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Localization of the gene encoding a neutral amino acid transporter-like protein to human chromosome band 19q13.3 and characterization of a simple sequence repeat DNA polymorphism.
    Jones EM; Menzel S; Espinosa R; Le Beau MM; Bell GI; Takeda J
    Genomics; 1994 Sep; 23(2):490-1. PubMed ID: 7835902
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel zinc finger cDNA with a polymorphic pentanucleotide repeat (ATTTT)n maps on human chromosome 19p.
    Chen H; Kalaitsidaki M; Warren AC; Avramopoulos D; Antonarakis SE
    Genomics; 1993 Mar; 15(3):621-5. PubMed ID: 8468057
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic distance of two fibrillar collagen loci, COL3A1 and COL5A2, located on the long arm of human chromosome 2.
    Tsipouras P; Schwartz RC; Liddell AC; Salkeld CS; Weil D; Ramirez F
    Genomics; 1988 Oct; 3(3):275-7. PubMed ID: 3224983
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic linkage mapping of the dehydroepiandrosterone sulfotransferase (STD) gene on the chromosome 19q13.3 region.
    Durocher F; Morissette J; Dufort I; Simard J; Luu-The V
    Genomics; 1995 Oct; 29(3):781-3. PubMed ID: 8575776
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A microsatellite-based multipoint index map of human chromosome 22.
    Buetow KH; Duggan D; Yang B; Ludwigsen S; Puck J; Porter J; Budarf M; Spielman R; Emanuel BS
    Genomics; 1993 Nov; 18(2):329-39. PubMed ID: 8288236
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic and physical map of 11 short tandem repeat polymorphisms on human chromosome 6.
    Wilkie PJ; Polymeropoulos MH; Trent JM; Small KW; Weber JL
    Genomics; 1993 Jan; 15(1):225-7. PubMed ID: 8432543
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22.
    Parolini O; Hejtmancik JF; Allen RC; Belmont JW; Lassiter GL; Henry MJ; Barker DF; Conley ME
    Genomics; 1993 Feb; 15(2):342-9. PubMed ID: 8449500
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular characterization of an intragenic minisatellite (VNTR) polymorphism in the human parathyroid hormone-related peptide gene in chromosome region 12p12.1-p11.2.
    Pausova Z; Morgan K; Fujiwara TM; Bourdon J; Goltzman D; Hendy GN
    Genomics; 1993 Jul; 17(1):243-4. PubMed ID: 8406461
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): localization to chromosome 2 and identification of a simple tandem repeat polymorphism.
    Stoffel M; Espinosa R; Powell KL; Philipson LH; Le Beau MM; Bell GI
    Genomics; 1994 May; 21(1):254-6. PubMed ID: 8088798
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Structure of the human type XIX collagen (COL19A1) gene, which suggests it has arisen from an ancestor gene of the FACIT family.
    Khaleduzzaman M; Sumiyoshi H; Ueki Y; Inoguchi K; Ninomiya Y; Yoshioka H
    Genomics; 1997 Oct; 45(2):304-12. PubMed ID: 9344653
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Regional localization of the human integrin beta 6 gene (ITGB6) to chromosome 2q24-q31.
    Fernández-Ruiz E; Sánchez-Madrid F
    Genomics; 1994 Jun; 21(3):638-40. PubMed ID: 7959743
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phosphoenolpyruvate carboxykinase (GTP): characterization of the human PCK1 gene and localization distal to MODY on chromosome 20.
    Ting CN; Burgess DL; Chamberlain JS; Keith TP; Falls K; Meisler MH
    Genomics; 1993 Jun; 16(3):698-706. PubMed ID: 8325643
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mapping of short tandem repeat polymorphisms on human chromosome 3.
    Wilkie PJ; Weber JL
    Genomics; 1994 Jan; 19(1):167-9. PubMed ID: 8188221
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The MLLT3 gene maps between D9S156 and D9S171 and contains an unstable polymorphic trinucleotide repeat.
    Walker GJ; Walters MK; Palmer JM; Hayward NK
    Genomics; 1994 Apr; 20(3):490-1. PubMed ID: 8034324
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.