BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

240 related articles for article (PubMed ID: 2991115)

  • 1. Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).
    Davies KE; Mattei MG; Mattei JF; Veenema H; McGlade S; Harper K; Tommerup N; Nielsen KB; Mikkelsen M; Beighton P
    Hum Genet; 1985; 70(3):249-55. PubMed ID: 2991115
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic heterogeneity of X-linked mental retardation with fragile X. Association of tight linkage to factor IX and incomplete penetrance in males.
    Giannelli F; Morris AH; Garrett C; Daker M; Thurston C; Smith CA
    Ann Hum Genet; 1987 May; 51(2):107-24. PubMed ID: 3674751
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.
    Oberlé I; Heilig R; Moisan JP; Kloepfer C; Mattéi GM; Mattéi JF; Boué J; Froster-Iskenius U; Jacobs PA; Lathrop GM
    Proc Natl Acad Sci U S A; 1986 Feb; 83(4):1016-20. PubMed ID: 3006023
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity.
    Brown WT; Gross AC; Chan CB; Jenkins EC
    Am J Med Genet; 1986; 23(1-2):643-64. PubMed ID: 3006490
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site.
    Szabo P; Purrello M; Rocchi M; Archidiacono N; Alhadeff B; Filippi G; Toniolo D; Martini G; Luzzatto L; Siniscalco M
    Proc Natl Acad Sci U S A; 1984 Dec; 81(24):7855-9. PubMed ID: 6595664
    [TBL] [Abstract][Full Text] [Related]  

  • 8. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.
    Davies KE
    Am J Med Genet; 1986; 23(1-2):633-42. PubMed ID: 3513572
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Linkage of nonspecific X-linked mental retardation to Xq21.31.
    Jedele KB; Michels VV; Schaid DJ; Schowalter KV; Thibodeau SN
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):436-42. PubMed ID: 1605223
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Linkage to Xq28 in a family with nonspecific X-linked mental retardation.
    Nordström AM; Penttinen M; von Koskull H
    Hum Genet; 1992 Nov; 90(3):263-6. PubMed ID: 1362558
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Gene for non-specific X-linked mental retardation maps in the pericentromeric region.
    Samanns C; Albrecht R; Neugebauer M; Neri G; Gal A
    Am J Med Genet; 1991; 38(2-3):224-7. PubMed ID: 2018062
    [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. Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male.
    Camerino G; Mattei MG; Mattei JF; Jaye M; Mandel JL
    Nature; 1983 Dec 15-21; 306(5944):701-4. PubMed ID: 6689201
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation.
    Hofker MH; Bergen AA; Skraastad MI; Carpenter NJ; Veenema H; Connor JM; Bakker E; van Ommen GJ; Pearson PL
    Am J Hum Genet; 1987 Apr; 40(4):312-28. PubMed ID: 2883888
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome.
    Suthers GK; Mulley JC; Voelckel MA; Dahl N; Väisänen ML; Steinbach P; Glass IA; Schwartz CE; van Oost BA; Thibodeau SN
    Am J Hum Genet; 1991 Mar; 48(3):460-7. PubMed ID: 1671806
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IX.
    Zoll B; Arnemann J; Krawczak M; Cooper DN; Pescia G; Wahli W; Steinbach P; Schmidtke J
    Hum Genet; 1985; 71(2):122-6. PubMed ID: 2995232
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.
    Connor JM; Pirrit LA; Yates JR; Crossley JA; Imrie SJ; Colgan JM
    J Med Genet; 1987 Jan; 24(1):14-22. PubMed ID: 2879932
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24.
    des Portes V; Soufir N; Carrié A; Billuart P; Bienvenu T; Vinet MC; Beldjord C; Ponsot G; Kahn A; Boué J; Chelly J
    Am J Med Genet; 1997 Oct; 72(3):324-8. PubMed ID: 9332663
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site.
    Mattei MG; Baeteman MA; Heilig R; Oberlé I; Davies K; Mandel JL; Mattei JF
    Hum Genet; 1985; 69(4):327-31. PubMed ID: 2985491
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.