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 *

151 related articles for article (PubMed ID: 2202564)

  • 21. [Mental retardation and the fragile X syndrome].
    Veenema H; Geraedts JP
    Ned Tijdschr Geneeskd; 1984 Mar; 128(13):618-21. PubMed ID: 6717630
    [No Abstract]   [Full Text] [Related]  

  • 22. Fragile-X syndrome. An overview.
    Scarbrough PR; Cosper P; Finley SC; Smith NB
    Ala J Med Sci; 1984 Jan; 21(1):68-72. PubMed ID: 6703250
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. [Spontaneous and induced chromosome instability in patients with fragile X syndrome].
    Suleĭmanova DG; Kuleshov NP
    Genetika; 1987 Mar; 23(3):504-9. PubMed ID: 3569895
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Encephalopathy linked to X chromosome fragility].
    Mattei JF
    Arch Fr Pediatr; 1982 Oct; 39(8):633-9. PubMed ID: 6760826
    [No Abstract]   [Full Text] [Related]  

  • 26. Fragile X-linked mental retardation, a new entity: case reports.
    Kelly TE; Shires MA; Harris L; Wyandt H; Wilson WG
    Va Med; 1983 Apr; 110(4):250-2. PubMed ID: 6868782
    [No Abstract]   [Full Text] [Related]  

  • 27. Fragile X transmission and the determination of carrier probabilities for genetic counseling.
    Mulley JC; Sutherland GR
    Am J Med Genet; 1987 Apr; 26(4):987-90. PubMed ID: 3591842
    [No Abstract]   [Full Text] [Related]  

  • 28. Detection of the fragile X chromosome and other fragile sites.
    Webb GC
    Clin Genet; 1985 May; 27(5):520-1. PubMed ID: 4006279
    [No Abstract]   [Full Text] [Related]  

  • 29. [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]  

  • 30. Fragile X syndrome: a common etiology of mental retardation.
    Rogers RC; Simensen RJ
    Am J Ment Defic; 1987 Mar; 91(5):445-9. PubMed ID: 3565490
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Expression of fragile site on the human X chromosome in somatic cell hybrids between human fragile X cells and thymidylate synthase-negative mouse mutant cells.
    Hori T; Ayusawa D; Glover TW; Seno T
    Jpn J Cancer Res; 1985 Oct; 76(10):977-83. PubMed ID: 3935628
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The fragile X syndrome.
    Brown WT
    Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [(Fra)X in male cousins with mental retardation].
    Rozynkowa D; Górski G; Jabłońska R
    Pediatr Pol; 1986 Jul; 61(7):441-5. PubMed ID: 3822610
    [No Abstract]   [Full Text] [Related]  

  • 34. [The fragile X chromosome syndrome].
    Seemanová E; Schmidt A; Subrt I; Macek M; Goetz P; Maríková T; Sulcová V
    Cesk Pediatr; 1987 Nov; 42(11):650-4. PubMed ID: 3427677
    [No Abstract]   [Full Text] [Related]  

  • 35. The fragile X syndrome: history, diagnosis, and treatment.
    Hagerman RJ; McBogg P; Hagerman PJ
    J Dev Behav Pediatr; 1983 Jun; 4(2):122-30. PubMed ID: 6348096
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [[Incidence of X-chromosome fragility in medium and severe mental retardation].
    Szakmáry E; Tomsits E; Vass M; Schuler D
    Orv Hetil; 1984 May; 125(20):1195-9. PubMed ID: 6718007
    [No Abstract]   [Full Text] [Related]  

  • 37. [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]  

  • 38. 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]  

  • 39. [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]  

  • 40. [Sex linked familial mental retardation with fragile X chromosome].
    Borochowitz Z; Dar H
    Harefuah; 1982 Aug; 103(3-4):67-8. PubMed ID: 7160768
    [No Abstract]   [Full Text] [Related]  

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