BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

322 related articles for article (PubMed ID: 25875842)

  • 1. Molecular diagnosis of Fragile X syndrome in subjects with intellectual disability of unknown origin: implications of its prevalence in regional Pakistan.
    Kanwal M; Alyas S; Afzal M; Mansoor A; Abbasi R; Tassone F; Malik S; Mazhar K
    PLoS One; 2015; 10(4):e0122213. PubMed ID: 25875842
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Frequency of FMR1 gene mutation and CGG repeat polymorphism in intellectually disabled children in Pakistan.
    Fatima T; Zaidi SA; Sarfraz N; Perween S; Khurshid F; Imtiaz F
    Am J Med Genet A; 2014 May; 164A(5):1151-61. PubMed ID: 24478267
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular diagnosis of fragile X syndrome using methylation sensitive techniques in a cohort of patients with intellectual disability.
    Chaudhary AG; Hussein IR; Abuzenadah A; Gari M; Bassiouni R; Sogaty S; Lary S; Al-Quaiti M; Al Balwi M; Al Qahtani M
    Pediatr Neurol; 2014 Apr; 50(4):368-76. PubMed ID: 24630283
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Unraveling unusual X-chromosome patterns during fragile-X syndrome genetic testing.
    Esposito G; Tremolaterra MR; Savarese M; Spiniello M; Patrizio MP; Lombardo B; Pastore L; Salvatore F; Carsana A
    Clin Chim Acta; 2018 Jan; 476():167-172. PubMed ID: 29170104
    [TBL] [Abstract][Full Text] [Related]  

  • 5. FMR1 gene mutations in patients with fragile X syndrome and obligate carriers: 30 years of experience in Chile.
    Santa María L; Aliaga S; Faundes V; Morales P; Pugin Á; Curotto B; Soto P; Peña MI; Salas I; Alliende MA
    Genet Res (Camb); 2016 Jun; 98():e11. PubMed ID: 27350105
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fragile X syndrome screening in Chinese children with unknown intellectual developmental disorder.
    Chen X; Wang J; Xie H; Zhou W; Wu Y; Wang J; Qin J; Guo J; Gu Q; Zhang X; Ji T; Zhang Y; Xiong Z; Wang L; Wu X; Latham GJ; Jiang Y
    BMC Pediatr; 2015 Jul; 15():77. PubMed ID: 26174701
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular screening of intellectually disabled patients and those with premature ovarian failure for CGG repeat expansion at FMR1 locus: Implication of combined triplet repeat primed polymerase chain reaction and methylation-specific polymerase chain reaction analysis.
    Muthuswamy S; Dean DD; Agarwal S
    Neurol India; 2016; 64(6):1175-1179. PubMed ID: 27841182
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Diagnostic testing in fragile X syndrome].
    Sireteanu A; Rusu C
    Rev Med Chir Soc Med Nat Iasi; 2006; 110(4):968-71. PubMed ID: 17438909
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndrome.
    Tzeng CC; Lin SJ; Chen YJ; Kuo PL; Jong YJ; Tsai LP; Chen RM
    Diagn Mol Pathol; 2001 Mar; 10(1):34-40. PubMed ID: 11277393
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical Genetic Testing for Fragile X Syndrome by Polymerase Chain Reaction Amplification and Southern Blot Analyses.
    Cai X; Arif M; Wan H; Kornreich R; Edelmann LJ
    Methods Mol Biol; 2019; 1942():11-27. PubMed ID: 30900172
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fragile X syndrome.
    Saldarriaga W; Tassone F; González-Teshima LY; Forero-Forero JV; Ayala-Zapata S; Hagerman R
    Colomb Med (Cali); 2014; 45(4):190-8. PubMed ID: 25767309
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Repeat expansion and methylation-sensitive triplet-primed polymerase chain reaction for fragile X mental retardation 1 gene screening in institutionalised intellectually disabled individuals.
    Sihombing NRB; Cai S; Wong DPW; Guan M; Chong SS; Faradz SMH; Winarni TI
    Singapore Med J; 2021 Mar; 62(3):143-148. PubMed ID: 31989181
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Coexistence of Fragile-X Syndrome, 8p23.1 Deletion, and Balanced Translocation t(7;10)(p10;q24) in a Single Family.
    Cortés H; Reyes-Rosales M; Rojas-Velasco AJ; García-Juárez B; Tapia-Guerrero YS; Arenas-Diaz S; Leyva-García N; Macías-Gallardo JJ; Carrillo-Mora P; Magaña JJ
    Genet Test Mol Biomarkers; 2020 Aug; 24(8):527-531. PubMed ID: 32716213
    [No Abstract]   [Full Text] [Related]  

  • 14. Molecular analysis of fragile X syndrome (FXS) among Malaysian patients with developmental disability.
    Ali EZ; Yakob Y; Md Desa N; Ishak T; Zakaria Z; Ngu LK; Keng WT
    Malays J Pathol; 2017 Aug; 39(2):99-106. PubMed ID: 28866690
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pilot fragile X screening in normal population of Taiwan.
    Tzeng CC; Cho WC; Kuo PL; Chen RM
    Diagn Mol Pathol; 1999 Sep; 8(3):152-6. PubMed ID: 10565687
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Standardization of capillary electrophoresis for diagnosis of fragile X syndrome in the Brazilian public health system.
    Gigonzac MA; Teodoro LS; Minasi LB; Vieira TC; da Cruz AD
    Electrophoresis; 2016 Dec; 37(23-24):3076-3078. PubMed ID: 27667322
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Establishment of FXS-A9 panel with a single human X chromosome from fragile X syndrome-associated individual.
    Nakayama Y; Adachi K; Shioda N; Maeta S; Nanba E; Kugoh H
    Exp Cell Res; 2021 Jan; 398(2):112419. PubMed ID: 33296661
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fragile X syndrome: a review of clinical and molecular diagnoses.
    Ciaccio C; Fontana L; Milani D; Tabano S; Miozzo M; Esposito S
    Ital J Pediatr; 2017 Apr; 43(1):39. PubMed ID: 28420439
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Diagnostic, carrier and prenatal genetic testing for fragile X syndrome and other FMR-1-related disorders in Johannesburg, South Africa: a 20-year review.
    Essop FB; Krause A
    S Afr Med J; 2013 Oct; 103(12 Suppl 1):994-8. PubMed ID: 24300646
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Simple molecular diagnostic method for fragile X syndrome in Egyptian patients: pilot study.
    Meguid NA; Ismail MF; El-Mahdy RS; Barakat MA; El-Awady MK
    Acta Biochim Pol; 2014; 61(2):259-63. PubMed ID: 24936518
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.