BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 11078558)

  • 1. Screening for the fragile X syndrome among mentally retarded males by hair root analysis.
    Tunçbilek E; Alikasifoğlu M; Aktas D; Duman F; Yanik H; Anar B; Oostra B; Willemsen R
    Am J Med Genet; 2000 Nov; 95(2):105-7. PubMed ID: 11078558
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome.
    Butler MG; Pratesi R; Vnencak-Jones CL
    J Intellect Disabil Res; 1995 Dec; 39 ( Pt 6)(Pt 6):544-53. PubMed ID: 8746743
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Screening with the FMR1 protein test among mentally retarded males.
    de Vries BB; Mohkamsing S; van den Ouweland AM; Halley DJ; Niermeijer MF; Oostra BA; Willemsen R
    Hum Genet; 1998 Oct; 103(4):520-2. PubMed ID: 9856500
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DNA testing for fragile X syndrome in 255 males from special schools in Singapore.
    Tan BS; Law HY; Zhao Y; Yoon CS; Ng IS
    Ann Acad Med Singap; 2000 Mar; 29(2):207-12. PubMed ID: 10895341
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Applicability of a checklist for clinical screening of the fragile X syndrome.
    Arvio M; Peippo M; Simola KO
    Clin Genet; 1997 Oct; 52(4):211-5. PubMed ID: 9383025
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group.
    de Vries BB; van den Ouweland AM; Mohkamsing S; Duivenvoorden HJ; Mol E; Gelsema K; van Rijn M; Halley DJ; Sandkuijl LA; Oostra BA; Tibben A; Niermeijer MF
    Am J Hum Genet; 1997 Sep; 61(3):660-7. PubMed ID: 9326332
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Noninvasive test for fragile X syndrome, using hair root analysis.
    Willemsen R; Anar B; De Diego Otero Y; de Vries BB; Hilhorst-Hofstee Y; Smits A; van Looveren E; Willems PJ; Galjaard H; Oostra BA
    Am J Hum Genet; 1999 Jul; 65(1):98-103. PubMed ID: 10364521
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [New methods for the diagnosis of fragile X syndrome: a study of the FMRP in blood and hair].
    Ramos-Fuentes FJ
    Rev Neurol; 2001 Oct; 33 Suppl 1():S9-S13. PubMed ID: 12447812
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males.
    Haddad LA; Mingroni-Netto RC; Vianna-Morgante AM; Pena SD
    Hum Genet; 1996 Jun; 97(6):808-12. PubMed ID: 8641701
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A step-wise diagnosis of fragile X syndrome in Taiwan.
    Huang YT; Chiang SC; Tzeng CC; Liu CH; Chien YH; Hwu WL
    Acta Paediatr Taiwan; 2004; 45(2):69-72. PubMed ID: 15335113
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [FMRP immunodetection on hair roots: application to the diagnosis of fragile X syndrome].
    Rifé Soler M; Sánchez Díaz A; Ramos F; Milà Recasens M
    An Pediatr (Barc); 2003 Nov; 59(5):431-5. PubMed ID: 14588214
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fragile X syndrome (review).
    Pimentel MM
    Int J Mol Med; 1999 Jun; 3(6):639-45. PubMed ID: 10341296
    [TBL] [Abstract][Full Text] [Related]  

  • 13. FMRP detection assay for the diagnosis of the fragile X syndrome.
    Willemsen R; Oostra BA
    Am J Med Genet; 2000; 97(3):183-8. PubMed ID: 11449486
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Screening for the fragile X syndrome among the mentally retarded: a clinical study. The Collaborative Fragile X Study Group.
    de Vries BB; Mohkamsing S; van den Ouweland AM; Mol E; Gelsema K; van Rijn M; Tibben A; Halley DJ; Duivenvoorden HJ; Oostra BA; Niermeijer MF
    J Med Genet; 1999 Jun; 36(6):467-70. PubMed ID: 10874635
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Non-invasive screening of fragile X syndrome A using urine and hair roots.
    Suwa K; Momoi MY
    Brain Dev; 2004 Sep; 26(6):380-3. PubMed ID: 15275700
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Hair root fragile X mental retardation protein assay for the diagnosis of fragile X syndrome].
    Luo XF; Zhong JM; Zhang XZ; Zou Y; Chen Y; Wu HP; Yu XY
    Zhongguo Dang Dai Er Ke Za Zhi; 2009 Oct; 11(10):817-20. PubMed ID: 19849940
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Diagnosis of the fragile X syndrome by the analysis of FMRP expression in blood and hair roots].
    Ramos FJ; Willemsen R
    Arch Pediatr; 2003 May; 10(5):401-2. PubMed ID: 12878331
    [No Abstract]   [Full Text] [Related]  

  • 18. FMRP expression studies in blood and hair roots in a fragile X family with methylation mosaics.
    de Vries BB; Severijnen LA; Jacobs A; Olmer R; Halley DJ; Oostra BA; Willemsen R
    J Med Genet; 2003 Jul; 40(7):535-9. PubMed ID: 12843328
    [No Abstract]   [Full Text] [Related]  

  • 19. [Molecular pathogenesis of fragile X syndrome].
    Sielska D; Milewski M; Bal J
    Med Wieku Rozwoj; 2002; 6(4):295-308. PubMed ID: 12810982
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A 15-item checklist for screening mentally retarded males for the fragile X syndrome.
    Butler MG; Mangrum T; Gupta R; Singh DN
    Clin Genet; 1991 May; 39(5):347-54. PubMed ID: 1860251
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.