BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

325 related articles for article (PubMed ID: 31469230)

  • 21. 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]  

  • 22. 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]  

  • 23. 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]  

  • 24. The clinical course of an overgrowth syndrome, from diagnosis in infancy through adulthood: the case of Beckwith-Wiedemann syndrome.
    Pappas JG
    Curr Probl Pediatr Adolesc Health Care; 2015 Apr; 45(4):112-7. PubMed ID: 25861997
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Diffuse infantile hepatic hemangiomas in a patient with Beckwith-Wiedemann syndrome: A new association?
    Macchiaiolo M; Markowich AH; Diociaiuti A; Gonfiantini MV; Buonuomo PS; Rana I; Monti L; El Hachem M; Bartuli A
    Am J Med Genet A; 2020 Aug; 182(8):1972-1976. PubMed ID: 32573107
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Adult experiences in Beckwith-Wiedemann syndrome.
    Drust WA; Mussa A; Gazzin A; Lapunzina P; Tenorio-Castaño J; Nevado J; Pascual P; Arias P; Parra A; Getz KD; Kalish JM
    Am J Med Genet C Semin Med Genet; 2023 Jun; 193(2):116-127. PubMed ID: 37163416
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Androgenetic chimerism as an etiology for Beckwith-Wiedemann syndrome: diagnosis and management.
    Sheppard SE; Lalonde E; Adzick NS; Beck AE; Bhatti T; De Leon DD; Duffy KA; Ganguly A; Hathaway E; Ji J; Linn R; Lord K; Randolph LM; Sajorda B; States L; Conlin LK; Kalish JM
    Genet Med; 2019 Nov; 21(11):2644-2649. PubMed ID: 31147633
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Beckwith-Wiedemann syndrome: multiple molecular mechanisms.
    Enklaar T; Zabel BU; Prawitt D
    Expert Rev Mol Med; 2006 Jul; 8(17):1-19. PubMed ID: 16842655
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Diagnosis and management of the phenotypic spectrum of twins with Beckwith-Wiedemann syndrome.
    Cohen JL; Duffy KA; Sajorda BJ; Hathaway ER; Gonzalez-Gandolfi CX; Richards-Yutz J; Gunter AT; Ganguly A; Kaplan J; Deardorff MA; Kalish JM
    Am J Med Genet A; 2019 Jul; 179(7):1139-1147. PubMed ID: 31067005
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Beckwith-Wiedemann syndrome.
    Weksberg R; Shuman C; Smith AC
    Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):12-23. PubMed ID: 16010676
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Beckwith-Wiedemann syndrome in diverse populations.
    Duffy KA; Sajorda BJ; Yu AC; Hathaway ER; Grand KL; Deardorff MA; Kalish JM
    Am J Med Genet A; 2019 Apr; 179(4):525-533. PubMed ID: 30719840
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Beckwith-Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature.
    Sassi H; Elaribi Y; Jilani H; Rejeb I; Hizem S; Sebai M; Kasdallah N; Bouthour H; Hannachi S; Beygo J; Saad A; Buiting K; H'mida Ben-Brahim D; BenJemaa L
    Mol Genet Genomic Med; 2021 Oct; 9(10):e1796. PubMed ID: 34510813
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature.
    Elefante P; Spedicati B; Faletra F; Pignata L; Cerrato F; Riccio A; Barbi E; Memo L; Travan L
    Ital J Pediatr; 2023 Sep; 49(1):127. PubMed ID: 37749604
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. 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]  

  • 36. Whole-exome sequencing reveals causative genetic variants for several overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrum.
    Higashimoto K; Sun F; Imagawa E; Saida K; Miyake N; Hara S; Yatsuki H; Kubiura-Ichimaru M; Fujita A; Mizuguchi T; Matsumoto N; Soejima H
    J Med Genet; 2024 Jan; ():. PubMed ID: 38228391
    [No Abstract]   [Full Text] [Related]  

  • 37. Diagnosis and Management of Beckwith-Wiedemann Syndrome.
    Wang KH; Kupa J; Duffy KA; Kalish JM
    Front Pediatr; 2019; 7():562. PubMed ID: 32039119
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith-Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesis.
    Bachmann N; Crazzolara R; Bohne F; Kotzot D; Maurer K; Enklaar T; Prawitt D; Bergmann C
    Pediatr Blood Cancer; 2017 Mar; 64(3):. PubMed ID: 27650505
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Colon hypoganglionosis in Beckwith-Wiedemann syndrome: a new rare comorbidity?
    Cazzaniga L; Parma B; Licini L; Dalla Rosa D; Cheli M; Selicorni A
    Clin Dysmorphol; 2022 Jan; 31(1):18-22. PubMed ID: 34561316
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Beckwith-Wiedemann syndrome: clinical and etiopathogenic aspects of a model genomic imprinting entity.
    Cammarata-Scalisi F; Avendaño A; Stock F; Callea M; Sparago A; Riccio A
    Arch Argent Pediatr; 2018 Oct; 116(5):368-373. PubMed ID: 30204990
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.