BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

257 related articles for article (PubMed ID: 1677599)

  • 1. No genetic linkage detected for schizophrenia to Xq27-q28.
    Delisi LE; Crow TJ; Davies KE; Terwilliger JD; Ott J; Ram R; Flint T; Boccio A
    Br J Psychiatry; 1991 May; 158():630-4. PubMed ID: 1677599
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Evidence for a pseudo-autosomal locus for schizophrenia using the method of affected sibling pairs.
    Collinge J; Delisi LE; Boccio A; Johnstone EC; Lane A; Larkin C; Leach M; Lofthouse R; Owen F; Poulter M
    Br J Psychiatry; 1991 May; 158():624-9. PubMed ID: 1860017
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.
    Oberlé I; Camerino G; Wrogemann K; Arveiler B; Hanauer A; Raimondi E; Mandel JL
    Hum Genet; 1987 Sep; 77(1):60-5. PubMed ID: 3502701
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.
    Voelckel MA; Philip N; Piquet C; Pellissier MC; Oberlé I; Birg F; Mattei MG; Mattei JF
    Hum Genet; 1989 Mar; 81(4):353-7. PubMed ID: 2564838
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.
    Arveiler B; Oberlé I; Vincent A; Hofker MH; Pearson PL; Mandel JL
    Am J Hum Genet; 1988 Feb; 42(2):380-9. PubMed ID: 2893549
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cytogenetic and physical mapping in the region of the X chromosome surrounding the fragile site.
    Nguyen C; Mattei MG; Rey JA; Baeteman MA; Mattei JF; Jordan BR
    Am J Med Genet; 1988; 30(1-2):601-11. PubMed ID: 2902799
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).
    Dahl N; Goonewardena P; Malmgren H; Gustavson KH; Holmgren G; Seemanova E; Annerén G; Flood A; Pettersson U
    Am J Hum Genet; 1989 Aug; 45(2):304-9. PubMed ID: 2569270
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Investigation by linkage analysis of the XY pseudoautosomal region in the genetic susceptibility to schizophrenia.
    Kalsi G; Curtis D; Brynjolfsson J; Butler R; Sharma T; Murphy P; Read T; Petursson H; Gurling HM
    Br J Psychiatry; 1995 Sep; 167(3):390-3. PubMed ID: 7496650
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Schizophrenia and sex chromosome anomalies.
    DeLisi LE; Friedrich U; Wahlstrom J; Boccio-Smith A; Forsman A; Eklund K; Crow TJ
    Schizophr Bull; 1994; 20(3):495-505. PubMed ID: 7973466
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A linkage study of schizophrenia to markers within Xp11 near the MAOB gene.
    Dann J; DeLisi LE; Devoto M; Laval S; Nancarrow DJ; Shields G; Smith A; Loftus J; Peterson P; Vita A; Comazzi M; Invernizzi G; Levinson DF; Wildenauer D; Mowry BJ; Collier D; Powell J; Crowe RR; Andreasen NC; Silverman JM; Mohs RC; Murray RM; Walters MK; Lennon DP; Crow TJ
    Psychiatry Res; 1997 May; 70(3):131-43. PubMed ID: 9211575
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An examination of linkage of schizophrenia and schizoaffective disorder to the pseudoautosomal region (Xp22.3).
    Crow TJ; Delisi LE; Lofthouse R; Poulter M; Lehner T; Bass N; Shah T; Walsh C; Boccio-Smith A; Shields G
    Br J Psychiatry; 1994 Feb; 164(2):159-64. PubMed ID: 7818635
    [TBL] [Abstract][Full Text] [Related]  

  • 12. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.
    Goonewardena P; Dahl N; Gustavson KH; Holmgren G; Pettersson U
    Ups J Med Sci Suppl; 1987; 44():155-64. PubMed ID: 2895524
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.
    Veenema H; Carpenter NJ; Bakker E; Hofker MH; Ward AM; Pearson PL
    J Med Genet; 1987 Jul; 24(7):413-21. PubMed ID: 2886667
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.
    Mulligan LM; Phillips MA; Forster-Gibson CJ; Beckett J; Partington MW; Simpson NE; Holden JJ; White BN
    Am J Hum Genet; 1985 May; 37(3):463-72. PubMed ID: 2988332
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Linkage analysis of bipolar illness with X-chromosome DNA markers: a susceptibility gene in Xq27-q28 cannot be excluded.
    De bruyn A; Raeymaekers P; Mendelbaum K; Sandkuijl LA; Raes G; Delvenne V; Hirsch D; Staner L; Mendlewicz J; Van Broeckhoven C
    Am J Med Genet; 1994 Dec; 54(4):411-9. PubMed ID: 7726217
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pulsed-field gel mapping studies in the vicinity of the fragile site at Xq27.3.
    Patterson M; Bell M; Schwartz C; Davies K
    Am J Med Genet; 1988; 30(1-2):581-91. PubMed ID: 3177471
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq.
    Buchanan JA; Buckton KE; Gosden CM; Newton MS; Clayton JF; Christie S; Hastie N
    Hum Genet; 1987 Jun; 76(2):165-72. PubMed ID: 3038730
    [TBL] [Abstract][Full Text] [Related]  

  • 18. New polymorphic DNA marker close to the fragile site FRAXA.
    Oostra BA; Hupkes PE; Perdon LF; van Bennekom CA; Bakker E; Halley DJ; Schmidt M; Du Sart D; Smits A; Wieringa B
    Genomics; 1990 Jan; 6(1):129-32. PubMed ID: 1968042
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Linkage studies in a large fragile X family.
    Patterson M; Bell M; Kress W; Davies KE; Froster-Iskenius U
    Am J Hum Genet; 1988 Nov; 43(5):684-8. PubMed ID: 2903666
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus.
    Vincent A; Dahl N; Oberlé I; Hanauer A; Mandel JL; Malmgren H; Pettersson U
    Genomics; 1989 Nov; 5(4):797-801. PubMed ID: 2574147
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.