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 *

193 related articles for article (PubMed ID: 31694075)

  • 21. Implications of the
    Wheeler A; Raspa M; Hagerman R; Mailick M; Riley C
    Pediatrics; 2017 Jun; 139(Suppl 3):S172-S182. PubMed ID: 28814538
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Development of a novel, accurate, automated, rapid, high-throughput technique suitable for population-based carrier screening for Fragile X syndrome.
    Strom CM; Huang D; Li Y; Hantash FM; Rooke J; Potts SJ; Sun W
    Genet Med; 2007 Apr; 9(4):199-207. PubMed ID: 17438383
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Clinical Validation of Fragile X Syndrome Screening by DNA Methylation Array.
    Schenkel LC; Schwartz C; Skinner C; Rodenhiser DI; Ainsworth PJ; Pare G; Sadikovic B
    J Mol Diagn; 2016 Nov; 18(6):834-841. PubMed ID: 27585064
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Identification of fragile X pre-mutation carriers in the Chinese obstetric population using a robust FMR1 polymerase chain reaction assay: implications for screening and prenatal diagnosis.
    Cheng YK; Lin CS; Kwok YK; Chan YM; Lau TK; Leung TY; Choy KW
    Hong Kong Med J; 2017 Apr; 23(2):110-6. PubMed ID: 28253484
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Reciprocal changes in DNA methylation and hydroxymethylation and a broad repressive epigenetic switch characterize FMR1 transcriptional silencing in fragile X syndrome.
    Brasa S; Mueller A; Jacquemont S; Hahne F; Rozenberg I; Peters T; He Y; McCormack C; Gasparini F; Chibout SD; Grenet O; Moggs J; Gomez-Mancilla B; Terranova R
    Clin Epigenetics; 2016; 8():15. PubMed ID: 26855684
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Fragile X syndrome: An overview and update of the FMR1 gene.
    Mila M; Alvarez-Mora MI; Madrigal I; Rodriguez-Revenga L
    Clin Genet; 2018 Feb; 93(2):197-205. PubMed ID: 28617938
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Fragile X molecular investigation and genetic counseling of intellectual disability/developmental delay patients in an Indian scenario.
    Dean DD; Agarwal S; Muthuswamy S
    Expert Rev Mol Diagn; 2019 Jul; 19(7):641-649. PubMed ID: 31159589
    [No Abstract]   [Full Text] [Related]  

  • 28. Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features.
    Baker EK; Arpone M; Aliaga SM; Bretherton L; Kraan CM; Bui M; Slater HR; Ling L; Francis D; Hunter MF; Elliott J; Rogers C; Field M; Cohen J; Cornish K; Santa Maria L; Faundes V; Curotto B; Morales P; Trigo C; Salas I; Alliende AM; Amor DJ; Godler DE
    Mol Autism; 2019; 10():21. PubMed ID: 31073396
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Ethical Dilemmas Linked to Fragile X Testing of Minors-a Preliminary Survey Among Professionals.
    Gabis LV; Shefer S; Raas-Rothschild A
    J Mol Neurosci; 2020 Feb; 70(2):254-259. PubMed ID: 31993931
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Results of carrier screening and prenatal diagnosis for FMR1 gene in 819 cases].
    Li J; Du J; Yang Q; Xu J; Li M; Fu H; Li M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Oct; 37(10):1104-1107. PubMed ID: 32924111
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Carrier diagnosis of the fragile X syndrome--a challenge in antenatal clinics.
    Ryynänen M; Kirkinen P; Mannermaa A; Saarikoski S
    Am J Obstet Gynecol; 1995 Apr; 172(4 Pt 1):1236-9. PubMed ID: 7726262
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Health problems in females carriers of premutation in the FMR1 gene.
    Lisik MZ
    Psychiatr Pol; 2017 Oct; 51(5):899-907. PubMed ID: 29289969
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Static and dynamic postural control deficits in aging fragile X mental retardation 1 (FMR1) gene premutation carriers.
    Wang Z; Khemani P; Schmitt LM; Lui S; Mosconi MW
    J Neurodev Disord; 2019 Jan; 11(1):2. PubMed ID: 30665341
    [TBL] [Abstract][Full Text] [Related]  

  • 34. An assessment of screening strategies for fragile X syndrome in the UK.
    Pembrey ME; Barnicoat AJ; Carmichael B; Bobrow M; Turner G
    Health Technol Assess; 2001; 5(7):1-95. PubMed ID: 11262423
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. A methylation PCR method determines
    Hadd AG; Filipovic-Sadic S; Zhou L; Williams A; Latham GJ; Berry-Kravis E; Hall DA
    Clin Epigenetics; 2016; 8():130. PubMed ID: 27980694
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Molecular testing for Fragile X Syndrome: lessons learned from 119,232 tests performed in a clinical laboratory.
    Strom CM; Crossley B; Redman JB; Buller A; Quan F; Peng M; McGinnis M; Fenwick RG; Sun W
    Genet Med; 2007 Jan; 9(1):46-51. PubMed ID: 17224689
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 10.