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 *

64 related articles for article (PubMed ID: 6231315)

  • 21. Some observations on the mental deficiency, normofunctional testicular hyperplasia and fra (X) (q28) chromosome syndrome.
    Rivera H; Hernandez A; Plascencia L; Sanchez-Corona J; Garcia-Cruz D; Cantu JM
    Ann Genet; 1981; 24(4):220-2. PubMed ID: 6977301
    [No Abstract]   [Full Text] [Related]  

  • 22. Clonal duplication of the Y chromosome and fra(X)(q28) in a case of epidermoid carcinoma of the esophagus.
    Casalone R; Minelli E; Portensoso P; Giudici A
    Cancer Genet Cytogenet; 1990 Apr; 45(2):269-71. PubMed ID: 2317776
    [No Abstract]   [Full Text] [Related]  

  • 23. "Fragile" X chromosome: major link to mental retardation.
    McBride G
    JAMA; 1981 Oct; 246(15):1631-2. PubMed ID: 7277637
    [No Abstract]   [Full Text] [Related]  

  • 24. Ultrastructure of the fragile X chromosome: new observations on the fragile site.
    Wen GY; Jenkins EC; Goldberg EM; Genovese M; Brown WT; Wisniewski HM
    Am J Med Genet; 1999 Apr; 83(4):331-3. PubMed ID: 10208174
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Cytogenetic techniques for the observation of chromosomes from the cultured cells of the blood and amniotic fluid].
    Yosida TH
    Gan To Kagaku Ryoho; 1985 Mar; 12(3 Pt 1):570-5. PubMed ID: 2408577
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Behavior of chromosome cores at heritable fragile sites: 16q22 and Xq27.
    Howard-Peebles PN; Howell WM
    Cytogenet Cell Genet; 1981; 31(2):115-9. PubMed ID: 7198024
    [No Abstract]   [Full Text] [Related]  

  • 27. First transmission electron micrograph of continuous mitotic spindle fibers between polar area and chromosome ends.
    Wen GY; Jenkins EC; Goldberg EM; Genovese M; Brown WT; Wisniewski HM
    Am J Med Genet; 1999 Apr; 83(4):334-7. PubMed ID: 10208175
    [No Abstract]   [Full Text] [Related]  

  • 28. Fragile X syndrome.
    Laxova R
    Adv Pediatr; 1994; 41():305-42. PubMed ID: 7992687
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Chromosome lesions which could be interpreted as "fragile sites" on the distal end of Xq.
    Butler MG; Allen GA; Haynes JL; Clark SJ
    Am J Med Genet; 1990 Oct; 37(2):250-3. PubMed ID: 2248293
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 12q13 fragility in a family with recurrent spontaneous abortions: expression of the fragile site under different culture conditions.
    Giardino D; Bettio D; Simoni G
    Ann Genet; 1990; 33(2):88-91. PubMed ID: 2241090
    [TBL] [Abstract][Full Text] [Related]  

  • 31. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.
    Goonewardena P; Dahl N; Gustavson KH; Holmgren G; Pettersson U
    Ups J Med Sci Suppl; 1987; 44():155-64. PubMed ID: 2895524
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Chromosome abnormalities and rare fragile sites detected in azoospermia patients.
    Seki N; Sumiya H; Shimazaki J; Toyama Y; Takahashi E; Murata M; Hori T
    Jpn J Hum Genet; 1992 Sep; 37(3):215-22. PubMed ID: 1472703
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Heritable fragile sites on human chromosomes: characterization of a new BrdU-dependent site in 12q24].
    Croci G; Manenti E; Caselli L
    Pathologica; 1983; 75 Suppl():324-8. PubMed ID: 6680435
    [No Abstract]   [Full Text] [Related]  

  • 34. [Prenatal diagnosis of a male fetal carrier of fragile X chromosome by the amniotic fluid cells].
    Tejada I; Boué J; Gilgenkrantz S
    Ann Genet; 1983; 26(4):247-50. PubMed ID: 6607707
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Chromosome characteristics of X-linked mental retardation. II. Autosomes].
    Bedel'baeva KhA; Baranovskaia LI; Zakharov AF
    Genetika; 1987 Mar; 23(3):510-20. PubMed ID: 3569896
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The fragile X syndrome I: familial variation in the proportion of lymphocytes with the fragile site in males.
    Soudek D; Partington MW; Lawson JS
    Am J Med Genet; 1984 Jan; 17(1):241-52. PubMed ID: 6711598
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Chromosome preparations from microplate cultures of man, dog, rat, and mouse.
    de Jong B; Anders GJ; van der Meer IH
    Hum Genet; 1976 Aug; 33(3):295-8. PubMed ID: 786851
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Mental retardation and fragile site Xq27-28: 2 affected brothers and their mother within the framework of chromosome instability].
    Tarantino E; Spagesi D; Simi P; Fiori B
    Pathologica; 1983; 75 Suppl():331-4. PubMed ID: 6680436
    [No Abstract]   [Full Text] [Related]  

  • 39. A technique for studying chemotaxis of leucocytes in well-defined chemotactic fields.
    Grimes GJ; Barnes FS
    Exp Cell Res; 1973 Jun; 79(2):375-85. PubMed ID: 4361082
    [No Abstract]   [Full Text] [Related]  

  • 40. Large scale culturing of normal diploid cells on glass beads using a novel type of culture vessel.
    Wöhler W; Rüdiger HW; Passarge E
    Exp Cell Res; 1972 Oct; 74(2):571-3. PubMed ID: 4562839
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.