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.
288 related articles for article (PubMed ID: 32349794)
41. Usefulness of the MS-MLPA technique in the diagnosis of Beckwith-Wiedemann syndrome and Silver-Russell syndrome. Acosta-Fernández E; Corona-Rivera JR; Ríos-Flores IM; Torres-Anguiano E; Corona-Rivera A; Peña-Padilla C; Bobadilla-Morales L Gac Med Mex; 2022; 158(4):202-209. PubMed ID: 36256576 [TBL] [Abstract][Full Text] [Related]
42. New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome. Smith AC; Rubin T; Shuman C; Estabrooks L; Aylsworth AS; McDonald MT; Steele L; Ray PN; Weksberg R Cytogenet Genome Res; 2006; 113(1-4):313-7. PubMed ID: 16575195 [TBL] [Abstract][Full Text] [Related]
43. A patient with multilocus imprinting disturbance involving hypomethylation at 11p15 and 14q32, and phenotypic features of Beckwith-Wiedemann and Temple syndromes. Grosvenor SE; Davies JH; Lever M; Sillibourne J; Mackay DJG; Temple IK Am J Med Genet A; 2022 Jun; 188(6):1896-1903. PubMed ID: 35266280 [TBL] [Abstract][Full Text] [Related]
44. Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith-Wiedemann Syndrome: Clinical Spectrum and Functional Characterization. Brioude F; Netchine I; Praz F; Le Jule M; Calmel C; Lacombe D; Edery P; Catala M; Odent S; Isidor B; Lyonnet S; Sigaudy S; Leheup B; Audebert-Bellanger S; Burglen L; Giuliano F; Alessandri JL; Cormier-Daire V; Laffargue F; Blesson S; Coupier I; Lespinasse J; Blanchet P; Boute O; Baumann C; Polak M; Doray B; Verloes A; Viot G; Le Bouc Y; Rossignol S Hum Mutat; 2015 Sep; 36(9):894-902. PubMed ID: 26077438 [TBL] [Abstract][Full Text] [Related]
45. 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]
47. Beckwith-Wiedemann syndrome: growth pattern and tumor risk according to molecular mechanism, and guidelines for tumor surveillance. Brioude F; Lacoste A; Netchine I; Vazquez MP; Auber F; Audry G; Gauthier-Villars M; Brugieres L; Gicquel C; Le Bouc Y; Rossignol S Horm Res Paediatr; 2013; 80(6):457-65. PubMed ID: 24335096 [TBL] [Abstract][Full Text] [Related]
48. 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]
49. Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15: few clinical features suggestive of Beckwith-Wiedemann syndrome. Adachi H; Takahashi I; Higashimoto K; Tsuchida S; Noguchi A; Tamura H; Arai H; Ito T; Masue M; Nishibori H; Takahashi T; Soejima H Endocr J; 2013; 60(4):403-8. PubMed ID: 23197114 [TBL] [Abstract][Full Text] [Related]
50. Development of disease-specific growth charts for Korean children with Beckwith-Wiedemann syndrome. Choi N; Kim HY; Ko JM Clin Genet; 2024 May; 105(5):533-542. PubMed ID: 38265109 [TBL] [Abstract][Full Text] [Related]
51. Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important. Eggermann T; Brück J; Knopp C; Fekete G; Kratz C; Tasic V; Kurth I; Elbracht M; Eggermann K; Begemann M J Mol Med (Berl); 2020 Oct; 98(10):1447-1455. PubMed ID: 32839827 [TBL] [Abstract][Full Text] [Related]
52. Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith-Wiedemann syndrome. Kalish JM; Boodhansingh KE; Bhatti TR; Ganguly A; Conlin LK; Becker SA; Givler S; Mighion L; Palladino AA; Adzick NS; De León DD; Stanley CA; Deardorff MA J Med Genet; 2016 Jan; 53(1):53-61. PubMed ID: 26545876 [TBL] [Abstract][Full Text] [Related]
53. 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]
54. Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects. DeBaun MR; Niemitz EL; McNeil DE; Brandenburg SA; Lee MP; Feinberg AP Am J Hum Genet; 2002 Mar; 70(3):604-11. PubMed ID: 11813134 [TBL] [Abstract][Full Text] [Related]
55. 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]
56. Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases. Bedeschi MF; Calvello M; Paganini L; Pezzani L; Baccarin M; Fontana L; Sirchia SM; Guerneri S; Canazza L; Leva E; Colombo L; Lalatta F; Mosca F; Tabano S; Miozzo M BMC Med Genet; 2017 Oct; 18(1):115. PubMed ID: 29047350 [TBL] [Abstract][Full Text] [Related]
57. Wilms tumour in Beckwith-Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines. Brzezinski J; Shuman C; Choufani S; Ray P; Stavropoulos DJ; Basran R; Steele L; Parkinson N; Grant R; Thorner P; Lorenzo A; Weksberg R Eur J Hum Genet; 2017 Sep; 25(9):1031-1039. PubMed ID: 28699632 [TBL] [Abstract][Full Text] [Related]
58. Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome. Abi Habib W; Azzi S; Brioude F; Steunou V; Thibaud N; Das Neves C; Le Jule M; Chantot-Bastaraud S; Keren B; Lyonnet S; Michot C; Rossi M; Pasquier L; Gicquel C; Rossignol S; Le Bouc Y; Netchine I Hum Mol Genet; 2014 Nov; 23(21):5763-73. PubMed ID: 24916376 [TBL] [Abstract][Full Text] [Related]
59. Beckwith-Wiedemann syndrome in sibs discordant for IC2 methylation. Niederhoffer KY; Peñaherrera M; Pugash D; Rupps R; Arbour L; Tessier F; Choufani S; Zhao C; Manokhina I; Shuman C; Robinson WP; Weksberg R; Boerkoel CF Am J Med Genet A; 2012 Jul; 158A(7):1662-9. PubMed ID: 22615066 [TBL] [Abstract][Full Text] [Related]
60. Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome. Reik W; Brown KW; Slatter RE; Sartori P; Elliott M; Maher ER Hum Mol Genet; 1994 Aug; 3(8):1297-301. PubMed ID: 7987305 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]