BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

52 related articles for article (PubMed ID: 1414622)

  • 1. Linkage studies in 16 St. Louis families. Present status and pursuit of an adjunct strategy.
    Devor EJ
    Adv Neurol; 1992; 58():181-7. PubMed ID: 1414622
    [No Abstract]   [Full Text] [Related]  

  • 2. Application of microsatellite DNA polymorphisms to linkage mapping of Tourette syndrome gene(s).
    Wilkie PJ; Ahmann PA; Hardacre J; LaPlant RJ; Hiner BC; Weber JL
    Adv Neurol; 1992; 58():173-80. PubMed ID: 1357938
    [No Abstract]   [Full Text] [Related]  

  • 3. The dopamine transporter protein gene (SLC6A3): primary linkage mapping and linkage studies in Tourette syndrome.
    Gelernter J; Vandenbergh D; Kruger SD; Pauls DL; Kurlan R; Pakstis AJ; Kidd KK; Uhl G
    Genomics; 1995 Dec; 30(3):459-63. PubMed ID: 8825631
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic study on Tourette syndrome in The Netherlands.
    Heutink P; van de Wetering BJ; Breedveld GJ; Oostra BA
    Adv Neurol; 1992; 58():167-72. PubMed ID: 1414621
    [No Abstract]   [Full Text] [Related]  

  • 5. Linkage study of the dopamine D5 receptor gene and Gilles de la Tourette syndrome.
    Barr CL; Wigg KG; Zovko E; Sandor P; Tsui LC
    Am J Med Genet; 1997 Feb; 74(1):58-61. PubMed ID: 9034008
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The genetic susceptibility to Gilles de la Tourette syndrome in a large multiple affected British kindred: linkage analysis excludes a role for the genes coding for dopamine D1, D2, D3, D4, D5 receptors, dopamine beta hydroxylase, tyrosinase, and tyrosine hydroxylase.
    Brett PM; Curtis D; Robertson MM; Gurling HM
    Biol Psychiatry; 1995 Apr; 37(8):533-40. PubMed ID: 7619976
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Alternative hypotheses on the inheritance of Tourette syndrome.
    Comings DE; Comings BG
    Adv Neurol; 1992; 58():189-99. PubMed ID: 1414623
    [No Abstract]   [Full Text] [Related]  

  • 8. Tourette symptoms in 161 related family members.
    McMahon WM; Leppert M; Filloux F; van de Wetering BJ; Hasstedt S
    Adv Neurol; 1992; 58():159-65. PubMed ID: 1414620
    [No Abstract]   [Full Text] [Related]  

  • 9. Hypothesis: homozygosity in Tourette syndrome.
    Comings DE; Comings BG; Knell E
    Am J Med Genet; 1989 Nov; 34(3):413-21. PubMed ID: 2596529
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A genome-wide scan and fine mapping in Tourette syndrome families.
    Pauls DL
    Adv Neurol; 2006; 99():130-5. PubMed ID: 16536358
    [No Abstract]   [Full Text] [Related]  

  • 11. Issues in genetic linkage studies of Tourette syndrome. Phenotypic spectrum and genetic model parameters.
    Pauls DL
    Adv Neurol; 1992; 58():151-7. PubMed ID: 1414619
    [No Abstract]   [Full Text] [Related]  

  • 12. Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndrome.
    Matsumoto N; David DE; Johnson EW; Konecki D; Burmester JK; Ledbetter DH; Weber JL
    Eur J Hum Genet; 2000 Nov; 8(11):875-83. PubMed ID: 11093278
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Genetic linkage analysis of Gilles de la Tourette Syndrome in a Colombian family].
    García-Cerén JJ; Valencia-Duarte AV; Cornejo JW; Carrizosa J; Cuartas JM; Zuluaga-Espinosa NA; Bedoya G; Ruiz-Linares A
    Rev Neurol; 2006 Feb 16-28; 42(4):211-6. PubMed ID: 16521059
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neuroreceptor subunit genes and the genetic susceptibility to Gilles de la Tourette syndrome.
    Brett PM; Curtis D; Robertson MM; Gurling HM
    Biol Psychiatry; 1997 Nov; 42(10):941-7. PubMed ID: 9359981
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers.
    Rosen DR; Sapp P; O'Regan J; McKenna-Yasek D; Schlumpf KS; Haines JL; Gusella JF; Horvitz HR; Brown RH
    Am J Med Genet; 1994 May; 51(1):61-9. PubMed ID: 7913294
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Gilles de la Tourette syndrome: a principal component factor analytic study of a large pedigree.
    Robertson MM; Cavanna AE
    Psychiatr Genet; 2007 Jun; 17(3):143-52. PubMed ID: 17417057
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A high-resolution linkage map of human 9q34.1.
    Henske EP; Ozelius L; Gusella JF; Haines JL; Kwiatkowski DJ
    Genomics; 1993 Sep; 17(3):587-91. PubMed ID: 8244374
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO.
    Griffith AJ; Burgess DL; Kohrman DC; Yu J; Blaschak J; Blanton SH; Boehnke M; Hecht JT; Overhauser J; Meisler MH
    Genomics; 1996 Jun; 34(3):299-303. PubMed ID: 8786128
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p.
    Antignac C; Arduy CH; Beckmann JS; Benessy F; Gros F; Medhioub M; Hildebrandt F; Dufier JL; Kleinknecht C; Broyer M
    Nat Genet; 1993 Apr; 3(4):342-5. PubMed ID: 7981755
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic and clinical analysis of a large Dutch Gilles de la Tourette family.
    Verkerk AJ; Cath DC; van der Linde HC; Both J; Heutink P; Breedveld G; Aulchenko YS; Oostra BA
    Mol Psychiatry; 2006 Oct; 11(10):954-64. PubMed ID: 16894393
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.