BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

285 related articles for article (PubMed ID: 27965001)

  • 61. Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith-Wiedemann progeny.
    Tannorella P; Calzari L; Daolio C; Mainini E; Vimercati A; Gentilini D; Soli F; Pedrolli A; Bonati MT; Larizza L; Russo S
    Clin Epigenetics; 2022 Mar; 14(1):43. PubMed ID: 35317853
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci.
    Azzi S; Rossignol S; Steunou V; Sas T; Thibaud N; Danton F; Le Jule M; Heinrichs C; Cabrol S; Gicquel C; Le Bouc Y; Netchine I
    Hum Mol Genet; 2009 Dec; 18(24):4724-33. PubMed ID: 19755383
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Investigation of a pervasive immune, cardiac, and behavioral phenotype in Beckwith-Wiedemann syndrome: A case report.
    McElroy TD; Duffy KA; Hathaway ER; Byrne ME; Kalish JM
    Am J Med Genet A; 2023 Apr; 191(4):1107-1110. PubMed ID: 36595472
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinism.
    Christesen HT; Christensen LG; Löfgren ÅM; Brøndum-Nielsen K; Svensson J; Brusgaard K; Samuelsson S; Elfving M; Jonson T; Grønskov K; Rasmussen L; Backman T; Hansen LK; Larsen AR; Petersen H; Detlefsen S
    Eur J Med Genet; 2020 Jan; 63(1):103632. PubMed ID: 30797057
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Desmoplastic nested spindle cell tumours and nested stromal epithelial tumours of the liver.
    Misra S; Bihari C
    APMIS; 2016 Apr; 124(4):245-51. PubMed ID: 26994733
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome.
    Squire JA; Li M; Perlikowski S; Fei YL; Bayani J; Zhang ZM; Weksberg R
    Genomics; 2000 May; 65(3):234-42. PubMed ID: 10857747
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Giant breast tumors in a patient with Beckwith-Wiedemann syndrome.
    Cappuccio G; De Crescenzo A; Ciancia G; Canta L; Moio M; Mataro I; Varone V; Pettinato G; Palumbo O; Carella M; Riccio A; Brunetti-Pierri N
    Am J Med Genet A; 2014 Jan; 164A(1):182-5. PubMed ID: 24214456
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome.
    Little MH; Thomson DB; Hayward NK; Smith PJ
    Hum Genet; 1988 Jun; 79(2):186-9. PubMed ID: 2839410
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Living donor liver transplantation for hepatoblastoma with Beckwith-Wiedemann syndrome.
    Sasaki K; Kasahara M; Fukuda A; Shigeta T; Tanaka H; Nakagawa S; Mitsui K; Harada R; Nakagawa A
    Pediatr Transplant; 2010 Nov; 14(7):E89-92. PubMed ID: 19496980
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor.
    Riccio A; Sparago A; Verde G; De Crescenzo A; Citro V; Cubellis MV; Ferrero GB; Silengo MC; Russo S; Larizza L; Cerrato F
    Endocr Dev; 2009; 14():1-9. PubMed ID: 19293570
    [TBL] [Abstract][Full Text] [Related]  

  • 71. 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]  

  • 72. Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma.
    Steenman M; Tomlinson G; Westerveld A; Mannens M
    Cytogenet Cell Genet; 1999; 86(2):157-61. PubMed ID: 10545709
    [TBL] [Abstract][Full Text] [Related]  

  • 73. [Beckwith-Wiedemann syndrome].
    Yoshiura K; Niikawa N
    Nihon Rinsho; 2000 Jul; 58(7):1511-4. PubMed ID: 10921333
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome.
    Weksberg R; Shen DR; Fei YL; Song QL; Squire J
    Nat Genet; 1993 Oct; 5(2):143-50. PubMed ID: 8252039
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Hepatoblastoma in an infant with Beckwith-Wiedemann Syndrome.
    Tsai SY; Jeng YM; Hwu WL; Ni YH; Chang MH; Wang TR
    J Formos Med Assoc; 1996 Feb; 95(2):180-3. PubMed ID: 9064012
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Epigenetic and genetic disturbance of the imprinted 11p15 region in Beckwith-Wiedemann and Silver-Russell syndromes.
    Demars J; Gicquel C
    Clin Genet; 2012 Apr; 81(4):350-61. PubMed ID: 22150955
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females.
    Moutou C; Junien C; Henry I; Bonaïti-Pellié C
    J Med Genet; 1992 Apr; 29(4):217-20. PubMed ID: 1583638
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Rapid detection of methylation change at H19 in human imprinting disorders using methylation-sensitive high-resolution melting.
    Wojdacz TK; Dobrovic A; Algar EM
    Hum Mutat; 2008 Oct; 29(10):1255-60. PubMed ID: 18473334
    [TBL] [Abstract][Full Text] [Related]  

  • 79. The utility of alpha-fetoprotein screening in Beckwith-Wiedemann syndrome.
    Duffy KA; Deardorff MA; Kalish JM
    Am J Med Genet A; 2017 Mar; 173(3):581-584. PubMed ID: 28160403
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Hepatoblastoma associated with Beckwith-Wiedemann syndrome and hemihypertrophy.
    Hamada Y; Takada K; Fukunaga S; Hioki K
    Pediatr Surg Int; 2003 Apr; 19(1-2):112-4. PubMed ID: 12721741
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.