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 *

153 related articles for article (PubMed ID: 3482420)

  • 21. Toward a physical map of the Xq28 region in man: linking color vision, G6PD, and coagulation factor VIII genes to an X-Y homology region.
    Arveiler B; Vincent A; Mandel JL
    Genomics; 1989 May; 4(4):460-71. PubMed ID: 2501212
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.
    Richards RI; Holman K; Kozman H; Kremer E; Lynch M; Pritchard M; Yu S; Mulley J; Sutherland GR
    J Med Genet; 1991 Dec; 28(12):818-23. PubMed ID: 1757956
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis.
    Vincent A; Heitz D; Petit C; Kretz C; Oberlé I; Mandel JL
    Nature; 1991 Feb; 349(6310):624-6. PubMed ID: 1672039
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage.
    Warren ST; Knight SJ; Peters JF; Stayton CL; Consalez GG; Zhang FP
    Proc Natl Acad Sci U S A; 1990 May; 87(10):3856-60. PubMed ID: 2339126
    [TBL] [Abstract][Full Text] [Related]  

  • 25. In situ hybridization studies using a molecular probe that maps to Xq27-Zq28.
    Duncan AM; Morgan C
    Hum Genet; 1990 Apr; 84(5):446-8. PubMed ID: 2323777
    [TBL] [Abstract][Full Text] [Related]  

  • 26. DNA linkage analysis of 26 families with fragile X syndrome.
    Carpenter NJ
    Am J Med Genet; 1991; 38(2-3):311-8. PubMed ID: 1673303
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Molecular analysis of a ring chromosome X in a family with fragile X syndrome.
    Mornet E; Bogyo A; Deluchat C; Simon-Bouy B; Mathieu M; Thépot F; Grisard MC; Leguern E; Boué J; Boué A
    Hum Genet; 1993 Oct; 92(4):373-8. PubMed ID: 8225318
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE.
    Hirst MC; Barnicoat A; Flynn G; Wang Q; Daker M; Buckle VJ; Davies KE; Bobrow M
    Hum Mol Genet; 1993 Feb; 2(2):197-200. PubMed ID: 8499907
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Pulsed-field gradient-gel studies around the fragile site.
    Dobkin CS; Brown WT
    Am J Med Genet; 1988; 30(1-2):593-600. PubMed ID: 2902798
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.
    Purrello M; Alhadeff B; Esposito D; Szabo P; Rocchi M; Truett M; Masiarz F; Siniscalco M
    EMBO J; 1985 Mar; 4(3):725-9. PubMed ID: 3924593
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome.
    Schmidt M; Certoma A; Du Sart D; Kalitsis P; Leversha M; Fowler K; Sheffield L; Jack I; Danks DM
    Hum Genet; 1990 Mar; 84(4):347-52. PubMed ID: 2307456
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Isolation of a human DNA sequence which spans the fragile X.
    Kremer EJ; Yu S; Pritchard M; Nagaraja R; Heitz D; Lynch M; Baker E; Hyland VJ; Little RD; Wada M
    Am J Hum Genet; 1991 Sep; 49(3):656-61. PubMed ID: 1882843
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines.
    Suthers GK; Hyland VJ; Callen DF; Oberle I; Rocchi M; Thomas NS; Morris CP; Schwartz CE; Schmidt M; Ropers HH
    Am J Hum Genet; 1990 Aug; 47(2):187-95. PubMed ID: 2378346
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. 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]  

  • 38. Linkage analysis of the fragile X syndrome using a new DNA marker U6.2 defining locus DXS304.
    Goonewardena P; Brown WT; Gross AC; Ferrando C; Dobkin C; Romano V; Bosco P; Ceratto N; Pettersson U; Dahl N
    Am J Med Genet; 1991; 38(2-3):322-7. PubMed ID: 1673305
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome.
    Bell MV; Hirst MC; Nakahori Y; MacKinnon RN; Roche A; Flint TJ; Jacobs PA; Tommerup N; Tranebjaerg L; Froster-Iskenius U
    Cell; 1991 Feb; 64(4):861-6. PubMed ID: 1997211
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.