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 *

167 related articles for article (PubMed ID: 11143494)

  • 1. A clinical checklist for fragile X syndrome: screening of Thai boys with developmental delay of unknown cause.
    Limprasert P; Ruangdaraganon N; Vasiknanonte P; Sura T; Jaruratanasirikul S; Sriwongpanich N; Sriplung H
    J Med Assoc Thai; 2000 Oct; 83(10):1260-6. PubMed ID: 11143494
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular screening for fragile X syndrome in Thailand.
    Limprasert P; Ruangdaraganon N; Sura T; Vasiknanonte P; Jinorose U
    Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():114-8. PubMed ID: 11400746
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Assessment of a clinical checklist in the diagnosis of fragile X syndrome in India.
    Guruju MR; Lavanya K; Thelma BK; Sujatha M; OmSai VR; Nagarathna V; Amarjyothi P; Jyothi A; Anandaraj MP
    J Clin Neurosci; 2009 Oct; 16(10):1305-10. PubMed ID: 19560928
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Effectiveness of a clinical test in the preselection of children with suspected fragile X syndrome].
    Fernández Carvajal I; Blanco Quirós A; Fernández Toral J; Tellería Orriols JJ; Alonso Ramos MJ; Sanz Cantalapiedra A; Martín Rodríguez JF; Palencia Luances R
    An Esp Pediatr; 2001 Apr; 54(4):326-30. PubMed ID: 11273815
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [A simplified six-item checklist for screening of fragile X syndrome].
    Guo Y; Chai J; Yao D; Zhang S; Huang S; Zhao S
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2000 Feb; 22(1):85-7. PubMed ID: 12903502
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fragile X syndrome: a clinico-genetic study of mentally retarded patients in Kuwait.
    Bastaki LA; Hegazy F; Al-Heneidi MM; Turki N; Azab AS; Naguib KK
    East Mediterr Health J; 2004; 10(1-2):116-24. PubMed ID: 16201716
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Haplotype analysis at the FRAXA locus in Thai subjects.
    Limprasert P; Saechan V; Ruangdaraganon N; Sura T; Vasiknanote P; Jaruratanasirikul S; Brown WT
    Am J Med Genet; 2001 Jan; 98(3):224-9. PubMed ID: 11169559
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prevalence and clinical characteristics of fragile X syndrome at child development clinic, Ramathibodi Hospital.
    Ruangdaraganon N; Limprasert P; Sura T; Sombuntham T; Sriwongpanich N; Kotchabhakdi N
    J Med Assoc Thai; 2000 Jan; 83(1):69-76. PubMed ID: 10710872
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation screening of the Aristaless-related homeobox (ARX) gene in Thai pediatric patients with delayed development: first report from Thailand.
    Rujirabanjerd S; Tongsippunyoo K; Sripo T; Limprasert P
    Eur J Med Genet; 2007; 50(5):346-54. PubMed ID: 17613295
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Evaluation of school children at high risk for fragile X syndrome utilizing buccal cell FMR-1 testing.
    Hagerman RJ; Wilson P; Staley LW; Lang KA; Fan T; Uhlhorn C; Jewell-Smart S; Hull C; Drisko J; Flom K
    Am J Med Genet; 1994 Jul; 51(4):474-81. PubMed ID: 7943023
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cognitive and behavioral profile of fragile X boys: correlations to molecular data.
    Backes M; Genç B; Schreck J; Doerfler W; Lehmkuhl G; von Gontard A
    Am J Med Genet; 2000 Nov; 95(2):150-6. PubMed ID: 11078566
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Diagnosis of fragile X syndrome].
    Glover G; Bernabé MJ; Carbonell P
    Rev Neurol; 2001 Oct; 33 Suppl 1():S6-9. PubMed ID: 12447811
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular screening for fragile X syndrome among Indonesian children with developmental disability.
    Faradz SM; Buckley M; Lam-Po-Tang ; Leigh D; Holden JJ
    Am J Med Genet; 1999 Apr; 83(4):350-1. PubMed ID: 10208179
    [No Abstract]   [Full Text] [Related]  

  • 15. [From gene to disease; fragile X-syndrome: hereditary mental retardation due to a developmental gene].
    de Vries LB; Oostra BA
    Ned Tijdschr Geneeskd; 2001 Mar; 145(10):474-6. PubMed ID: 11268909
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues.
    Mandel JL; Biancalana V
    Growth Horm IGF Res; 2004 Jun; 14 Suppl A():S158-65. PubMed ID: 15135801
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [Analysis of expression of FMR-1 gene in male patients with fragile X syndrome using RT-PCR].
    Zhu W; Li M; Zhao Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Feb; 15(1):17-9. PubMed ID: 9456366
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population.
    Pouya AR; Abedini SS; Mansoorian N; Behjati F; Nikzat N; Mohseni M; Nieh SE; Abbasi Moheb L; Darvish H; Monajemi GB; Banihashemi S; Kahrizi K; Ropers HH; Najmabadi H
    Eur J Med Genet; 2009; 52(4):170-3. PubMed ID: 19361583
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Health supervision for children with fragile X syndrome.
    Hersh JH; Saul RA;
    Pediatrics; 2011 May; 127(5):994-1006. PubMed ID: 21518720
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.