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 *

121 related articles for article (PubMed ID: 6399303)

  • 41. Fragile X syndrome.
    de la Cruz FF
    Am J Ment Defic; 1985 Sep; 90(2):119-23. PubMed ID: 3901755
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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]  

  • 43. A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation.
    Pembrey ME; Winter RM; Davies KE
    Am J Med Genet; 1985 Aug; 21(4):709-17. PubMed ID: 4040705
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.
    Blomquist HK; Gustavson KH; Holmgren G; Nordenson I; Pålsson-Stråe U
    Clin Genet; 1983 Dec; 24(6):393-8. PubMed ID: 6652951
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Interpretation of the heterogeneity in the linkage relationships of DNA markers around the fragile X locus.
    Winter R; Pembrey M
    Hum Genet; 1987 Nov; 77(3):297-8. PubMed ID: 3479389
    [No Abstract]   [Full Text] [Related]  

  • 46. Fragile-X mental retardation syndrome transmitted through intellectually normal males: implications for genetic counseling.
    Young RS; Jaramillo C; McCombs JL; Moore CM; Jorgenson RJ
    South Med J; 1986 Apr; 79(4):405-9. PubMed ID: 3704696
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. 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]  

  • 49. RFLP for linkage analysis of fragile X syndrome.
    Brown WT; Wu Y; Gross AC; Chan CB; Dobkin CS; Jenkins EC
    Lancet; 1987 Jan; 1(8527):280. PubMed ID: 2880102
    [No Abstract]   [Full Text] [Related]  

  • 50. 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]  

  • 51. Further evidence for genetic heterogeneity in the fragile X syndrome.
    Brown WT; Jenkins EC; Gross AC; Chan CB; Krawczun MS; Duncan CJ; Sklower SL; Fisch GS
    Hum Genet; 1987 Apr; 75(4):311-21. PubMed ID: 2883105
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Sex-related neurologic diseases. Familial X-linked mental retardation with a fragile X marker. Study of 8 families].
    Rodríguez Costa T; Gabarrón Llamas J; Casas Fernández C; Glover López G; Puche Mira A; Jiménez Cocina A
    An Esp Pediatr; 1984 Oct; 21 Suppl 20():54-7. PubMed ID: 6595955
    [No Abstract]   [Full Text] [Related]  

  • 53. 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]  

  • 54. Use of restriction fragment length polymorphism analysis for detecting carriers of "fragile X" syndrome.
    Thibodeau SN
    Clin Chem; 1987 Oct; 33(10):1726-30. PubMed ID: 2889542
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Genetic mapping of the human X chromosome: linkage analysis of the q26-q28 region that includes the fragile X locus and isolation of expressed sequences.
    Mandel JL; Arveiler B; Camerino G; Hanauer A; Heilig R; Koenig M; Oberlé I
    Cold Spring Harb Symp Quant Biol; 1986; 51 Pt 1():195-203. PubMed ID: 3472716
    [No Abstract]   [Full Text] [Related]  

  • 56. Prenatal diagnosis of X-linked mental retardation with fragile (X) using fetoscopy and fetal blood sampling.
    Webb T; Gosden CM; Rodeck CH; Hamill MA; Eason PE
    Prenat Diagn; 1983; 3(2):131-7. PubMed ID: 6622392
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [X chromosome-linked mental retardation with fragile X chromosome and macro-orchidism].
    Zollinger A; Schmid W; Vilan J; Sorg B; Knoblauch M
    Schweiz Med Wochenschr; 1983 Feb; 113(7):238-44. PubMed ID: 6836249
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [X-linked mental retardation, macro-orchism, and X chromosome fragile site. Presentation of 6 cases in 2 families].
    Pascual-Castroviejo I; López Pajares I; Delicado A
    An Esp Pediatr; 1982 Dec; 17(6):466-74. PubMed ID: 6892145
    [TBL] [Abstract][Full Text] [Related]  

  • 59. From hemophilia B to hemophilia A via the fragile X locus: genes and recombination in the distal region of the human X chromosome long arm.
    Oberlé I; Mandel JL
    Horiz Biochem Biophys; 1986; 8():51-89. PubMed ID: 2875934
    [No Abstract]   [Full Text] [Related]  

  • 60. An 18-locus linkage map of the pericentromeric region of the human X chromosome: genetic framework for mapping X-linked disorders.
    Mahtani MM; Lafrenière RG; Kruse TA; Willard HF
    Genomics; 1991 Aug; 10(4):849-57. PubMed ID: 1916819
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.