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 *

284 related articles for article (PubMed ID: 23917791)

  • 1. Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.
    Calvello M; Tabano S; Colapietro P; Maitz S; Pansa A; Augello C; Lalatta F; Gentilin B; Spreafico F; Calzari L; Perotti D; Larizza L; Russo S; Selicorni A; Sirchia SM; Miozzo M
    Epigenetics; 2013 Oct; 8(10):1053-60. PubMed ID: 23917791
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi.
    Paganini L; Carlessi N; Fontana L; Silipigni R; Motta S; Fiori S; Guerneri S; Lalatta F; Cereda A; Sirchia S; Miozzo M; Tabano S
    Epigenetics; 2015; 10(7):643-9. PubMed ID: 26061650
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith-Wiedemann syndrome.
    Lin HY; Chuang CK; Tu RY; Fang YY; Su YN; Chen CP; Chang CY; Liu HC; Chu TH; Niu DM; Lin SP
    Mol Genet Metab; 2016 Sep; 119(1-2):8-13. PubMed ID: 27436784
    [TBL] [Abstract][Full Text] [Related]  

  • 4. High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith-Wiedemann syndrome.
    Baskin B; Choufani S; Chen YA; Shuman C; Parkinson N; Lemyre E; Micheil Innes A; Stavropoulos DJ; Ray PN; Weksberg R
    Hum Genet; 2014 Mar; 133(3):321-30. PubMed ID: 24154661
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.
    Gaston V; Le Bouc Y; Soupre V; Burglen L; Donadieu J; Oro H; Audry G; Vazquez MP; Gicquel C
    Eur J Hum Genet; 2001 Jun; 9(6):409-18. PubMed ID: 11436121
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Epigenotype and phenotype correlations in patients with Beckwith-Wiedemann syndrome.
    Bilgin B; Kabaçam S; Taşkıran E; Şimşek-Kiper PÖ; Alanay Y; Boduroğlu K; Utine GE
    Turk J Pediatr; 2018; 60(5):506-513. PubMed ID: 30968633
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.
    Catchpoole D; Lam WW; Valler D; Temple IK; Joyce JA; Reik W; Schofield PN; Maher ER
    J Med Genet; 1997 May; 34(5):353-9. PubMed ID: 9152830
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Methylation analysis in tongue tissue of BWS patients identifies the (EPI)genetic cause in 3 patients with normal methylation levels in blood.
    Alders M; Maas SM; Kadouch DJ; van der Lip K; Bliek J; van der Horst CM; Mannens MM
    Eur J Med Genet; 2014; 57(6):293-7. PubMed ID: 24704790
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Epigenetic Abnormalities of 11p15.5 Region in Beckwith-Wiedemann Syndrome - A Report of Eight Indian Cases.
    Correa ARE; Mishra P; Kabra M; Gupta N
    Indian J Pediatr; 2020 Mar; 87(3):175-178. PubMed ID: 31997239
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.
    Engel JR; Smallwood A; Harper A; Higgins MJ; Oshimura M; Reik W; Schofield PN; Maher ER
    J Med Genet; 2000 Dec; 37(12):921-6. PubMed ID: 11106355
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Severe presentation of Beckwith-Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15.
    Smith AC; Shuman C; Chitayat D; Steele L; Ray PN; Bourgeois J; Weksberg R
    Am J Med Genet A; 2007 Dec; 143A(24):3010-5. PubMed ID: 18000906
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Deciphering Epigenetic Backgrounds in a Korean Cohort with Beckwith-Wiedemann Syndrome.
    Kim HY; Shin CH; Lee YA; Shin CH; Kim GH; Ko JM
    Ann Lab Med; 2022 Nov; 42(6):668-677. PubMed ID: 35765875
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol.
    Mussa A; Molinatto C; Baldassarre G; Riberi E; Russo S; Larizza L; Riccio A; Ferrero GB
    J Pediatr; 2016 Sep; 176():142-149.e1. PubMed ID: 27372391
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Beckwith-Wiedemann Syndrome.
    Lin HY; Lee CL; Fran S; Tu RY; Chang YH; Niu DM; Chang CY; Chiu PC; Chou YY; Hsiao HP; Yang CF; Tsai MC; Chu TH; Chuang CK; Lin SP
    J Pers Med; 2021 Oct; 11(11):. PubMed ID: 34834418
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.
    Slatter RE; Elliott M; Welham K; Carrera M; Schofield PN; Barton DE; Maher ER
    J Med Genet; 1994 Oct; 31(10):749-53. PubMed ID: 7837249
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.
    Weksberg R; Nishikawa J; Caluseriu O; Fei YL; Shuman C; Wei C; Steele L; Cameron J; Smith A; Ambus I; Li M; Ray PN; Sadowski P; Squire J
    Hum Mol Genet; 2001 Dec; 10(26):2989-3000. PubMed ID: 11751681
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1.
    Poole RL; Leith DJ; Docherty LE; Shmela ME; Gicquel C; Splitt M; Temple IK; Mackay DJ
    Eur J Hum Genet; 2012 Feb; 20(2):240-3. PubMed ID: 21863054
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
    Russo S; Calzari L; Mussa A; Mainini E; Cassina M; Di Candia S; Clementi M; Guzzetti S; Tabano S; Miozzo M; Sirchia S; Finelli P; Prontera P; Maitz S; Sorge G; Calcagno A; Maghnie M; Divizia MT; Melis D; Manfredini E; Ferrero GB; Pecile V; Larizza L
    Clin Epigenetics; 2016; 8():23. PubMed ID: 26933465
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Proposal for Practical Approach in Prenatal Diagnosis of Beckwith-Wiedemann Syndrome and Review of the Literature.
    Ma GC; Chen TH; Wu WJ; Lee DJ; Lin WH; Chen M
    Diagnostics (Basel); 2022 Jul; 12(7):. PubMed ID: 35885613
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 15.