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 *

150 related articles for article (PubMed ID: 3472716)

  • 41. Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation.
    Voelckel MA; Mattei MG; N'Guyen C; Philip N; Birg F; Mattei JF
    Hum Genet; 1988 Dec; 80(4):375-8. PubMed ID: 2904402
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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]  

  • 43. New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locus.
    Rousseau F; Vincent A; Oberlé I; Mandel JL
    Hum Genet; 1990 Feb; 84(3):263-6. PubMed ID: 1968034
    [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. Conference report: International Workshop on the fragile X and X-linked mental retardation.
    Opitz JM; Sutherland GR
    Am J Med Genet; 1984 Jan; 17(1):5-94. PubMed ID: 6369987
    [No Abstract]   [Full Text] [Related]  

  • 46. 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]  

  • 47. The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X.
    Sutherland GR; Baker E
    Clin Genet; 1990 Mar; 37(3):167-72. PubMed ID: 2323087
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. 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]  

  • 50. Hereditary unstable DNA: a new explanation for some old genetic questions?
    Sutherland GR; Haan EA; Kremer E; Lynch M; Pritchard M; Yu S; Richards RI
    Lancet; 1991 Aug; 338(8762):289-92. PubMed ID: 1677119
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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]  

  • 52. Linkage and recombination between fragile X-linked mental retardation and the factor IX gene.
    Warren ST; Glover TW; Davidson RL; Jagadeeswaran P
    Hum Genet; 1985; 69(1):44-6. PubMed ID: 3967889
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Deleted X chromosomes in patients with the fragile X syndrome.
    Fitchett M; Seabright M
    J Med Genet; 1984 Oct; 21(5):373. PubMed ID: 6542142
    [No Abstract]   [Full Text] [Related]  

  • 54. 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]  

  • 55. Concurrence of the triple-X syndrome and expression of the fragile site Xq27.3.
    Fuster C; Templado C; Miró R; Barrios L; Egozcue J
    Hum Genet; 1988 Mar; 78(3):293. PubMed ID: 3346020
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Macroorchidism and fragile X in mentally retarded males. Clinical, cytogenetic, and some hormonal investigations in mentally retarded males, including two with the fragile site at Xq28, fra(X)(q28).
    Nielsen KB; Tommerup N; Dyggve HV; Schou C
    Hum Genet; 1982; 61(2):113-7. PubMed ID: 6215327
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [The 47,XXX syndrome in a family with the fragile X chromosome syndrome].
    Seemanová E; Schmidt A; Subrt I; Passarge E; Macek M; Nedomová V
    Cas Lek Cesk; 1985 Aug; 124(31):988-91. PubMed ID: 4028081
    [No Abstract]   [Full Text] [Related]  

  • 58. [Encephalopathy related to X fragility: neither inactivation nor deletion of the distal fragment q28 to qter. Enzymatic and morphometric evidence].
    Jalbert H; Baeteman MA; Trochet-Royer C; Mattei MG; Mattei JF; Leroux D; Jalbert P
    J Genet Hum; 1983 Jun; 31(2):133-9. PubMed ID: 6631423
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Genetic aspects of fragile X syndrome].
    Hori T
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):1041-4. PubMed ID: 2908391
    [No Abstract]   [Full Text] [Related]  

  • 60. Fragile X syndrome: a unique mutation in man.
    Nussbaum RL; Ledbetter DH
    Annu Rev Genet; 1986; 20():109-45. PubMed ID: 3545058
    [No Abstract]   [Full Text] [Related]  

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