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 *

236 related articles for article (PubMed ID: 6955257)

  • 61. Non-specific X-linked mental retardation: background, types, diagnosis and prevalence.
    Howard-Peebles PN
    J Ment Defic Res; 1982 Dec; 26 (Pt 4)():205-13. PubMed ID: 6763078
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Familial X-linked mental retardation, verbal disability, and marker X chromosomes.
    Howard-Peebles PN; Stoddard GR; Mims MG
    Am J Hum Genet; 1979 Mar; 31(2):214-22. PubMed ID: 453204
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Possible erasure of the imprint on a fragile X chromosome when transmitted by a male.
    Laird CD
    Am J Med Genet; 1991; 38(2-3):391-5. PubMed ID: 2018078
    [TBL] [Abstract][Full Text] [Related]  

  • 64. A unique form of mental retardation with a distinctive phenotype maps to Xq26-q27.
    Shashi V; Berry MN; Shoaf S; Sciote JJ; Goldstein D; Hart TC
    Am J Hum Genet; 2000 Feb; 66(2):469-79. PubMed ID: 10677307
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Fragile X syndrome with extra microchromosome.
    López-Pajares I; Delicado A; Pascual-Castroviejo I; López-Martin V; Moreno F; Garcia-Marcos JA
    Clin Genet; 1994 Apr; 45(4):186-9. PubMed ID: 8062436
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Fra(X)(q27.2), the common fragile site, observed in only one of 760 cases studied for the fragile X syndrome.
    Jenkins EC; Genovese MJ; Duncan CJ; Gu H; Stark-Houck SL; Lele K; Li SY; Krawczun MS
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):136-41. PubMed ID: 1605182
    [TBL] [Abstract][Full Text] [Related]  

  • 67. [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]  

  • 68. Investigation of the segregation of the fragile X mutation in daughters of obligate carrier women.
    Sherman SL; Turner G; Robinson H; Laing S
    Am J Med Genet; 1988; 30(1-2):633-9. PubMed ID: 3177475
    [TBL] [Abstract][Full Text] [Related]  

  • 69. [Variability in the expression of the fragile site of the (fra)X chromosome in 2 consecutive cell cycles].
    Zakharov AF; Bedel'baeva KhA; Baranovskaia LI
    Biull Eksp Biol Med; 1986 Dec; 102(12):738-41. PubMed ID: 3801629
    [TBL] [Abstract][Full Text] [Related]  

  • 70. The fragile X(q27) form of X-linked mental retardation: FUdR as an inducing agent for fra(X)(q27) expression in lymphocytes, fibroblasts, and amniocytes.
    Brookwell R; Daniel A; Turner G; Fishburn J
    Am J Med Genet; 1982 Oct; 13(2):139-48. PubMed ID: 6215863
    [TBL] [Abstract][Full Text] [Related]  

  • 71. FRAXE and mental retardation.
    Mulley JC; Yu S; Loesch DZ; Hay DA; Donnelly A; Gedeon AK; Carbonell P; López I; Glover G; Gabarrón I
    J Med Genet; 1995 Mar; 32(3):162-9. PubMed ID: 7783162
    [TBL] [Abstract][Full Text] [Related]  

  • 72. [Fragile X chromosome and X-linked mental retardation (author's transl)].
    Fonatsch C; Flatz SD
    Wien Klin Wochenschr; 1982 Apr; 94(8):217-9. PubMed ID: 7101956
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Marker X-associated mental retardation. A study of 150 retarded males.
    Kähkönen M; Leisti J; Wilska M; Varonen S
    Clin Genet; 1983 Jun; 23(6):397-404. PubMed ID: 6576874
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Activity of the fragile X in heterozygous carriers.
    Uchida IA; Joyce EM
    Am J Hum Genet; 1982 Mar; 34(2):286-93. PubMed ID: 6176123
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Heritable fragility at 11q13 and 12q13.
    Smeets DF; Scheres JM; Hustinx TW
    Clin Genet; 1985 Aug; 28(2):145-50. PubMed ID: 4042396
    [TBL] [Abstract][Full Text] [Related]  

  • 76. X linked severe mental retardation, craniofacial dysmorphology, epilepsy, ophthalmoplegia, and cerebellar atrophy in a large South African kindred is localised to Xq24-q27.
    Christianson AL; Stevenson RE; van der Meyden CH; Pelser J; Theron FW; van Rensburg PL; Chandler M; Schwartz CE
    J Med Genet; 1999 Oct; 36(10):759-66. PubMed ID: 10528855
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Expression of folate-sensitive fragile sites in lymphocyte chromosomes.
    Fuster C; Miró R; Templado C; Barrios L; Egozcue J
    Hum Genet; 1989 Feb; 81(3):243-6. PubMed ID: 2921033
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male.
    Camerino G; Mattei MG; Mattei JF; Jaye M; Mandel JL
    Nature; 1983 Dec 15-21; 306(5944):701-4. PubMed ID: 6689201
    [TBL] [Abstract][Full Text] [Related]  

  • 79. 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]  

  • 80. Expression of the autosomal folate-sensitive fragile sites in ten kindreds with Martin-Bell syndrome.
    Ventruto V; Stabile M; Gentile G; de Tollis G; Colantuoni M; Sirone P; Perone L; Lonardo F; Della Monica M; Fiore M
    Ann Genet; 1986; 29(1):59-61. PubMed ID: 3487280
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.