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.
132 related articles for article (PubMed ID: 34098225)
21. Epigenetic Characterization of CDKN1C in Placenta Samples from Non-syndromic Intrauterine Growth Restriction. López-Abad M; Iglesias-Platas I; Monk D Front Genet; 2016; 7():62. PubMed ID: 27200075 [TBL] [Abstract][Full Text] [Related]
22. Beckwith-Wiedemann syndrome: historical, clinicopathological, and etiopathogenetic perspectives. Cohen MM Pediatr Dev Pathol; 2005; 8(3):287-304. PubMed ID: 16010495 [TBL] [Abstract][Full Text] [Related]
23. Evaluation of the abdominopelvic region using MRI in patients with primary amenorrhea. Gündoğdu E; Emekli E; Oğuzman M; Kebapçı M J Pediatr Endocrinol Metab; 2019 Sep; 32(9):995-1003. PubMed ID: 31369396 [TBL] [Abstract][Full Text] [Related]
24. An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome. Hatada I; Ohashi H; Fukushima Y; Kaneko Y; Inoue M; Komoto Y; Okada A; Ohishi S; Nabetani A; Morisaki H; Nakayama M; Niikawa N; Mukai T Nat Genet; 1996 Oct; 14(2):171-3. PubMed ID: 8841187 [TBL] [Abstract][Full Text] [Related]
25. Brain abnormalities in patients with Beckwith-Wiedemann syndrome. Gardiner K; Chitayat D; Choufani S; Shuman C; Blaser S; Terespolsky D; Farrell S; Reiss R; Wodak S; Pu S; Ray PN; Baskin B; Weksberg R Am J Med Genet A; 2012 Jun; 158A(6):1388-94. PubMed ID: 22585446 [TBL] [Abstract][Full Text] [Related]
26. Acute lymphocytic leukaemia in a child with Beckwith-Wiedemann syndrome harbouring a CDKN1C mutation. Abadie C; Bernard F; Netchine I; Sanlaville D; Roque A; Rossignol S; Coupier I Eur J Med Genet; 2010; 53(6):400-3. PubMed ID: 20826236 [TBL] [Abstract][Full Text] [Related]
27. 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]
28. IMAGe, a new clinical association of intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies. Vilain E; Le Merrer M; Lecointre C; Desangles F; Kay MA; Maroteaux P; McCabe ER J Clin Endocrinol Metab; 1999 Dec; 84(12):4335-40. PubMed ID: 10599684 [TBL] [Abstract][Full Text] [Related]
29. Rare clinical findings in three sporadic cases of Beckwith-Wiedemann syndrome due to novel mutations in the CDKN1C gene. Jurkiewicz D; Skórka A; Ciara E; Kugaudo M; Pelc M; Chrzanowska K; Krajewska-Walasek M Clin Dysmorphol; 2020 Jan; 29(1):28-34. PubMed ID: 31804259 [TBL] [Abstract][Full Text] [Related]
30. Epigenetic anomalies in childhood growth disorders. Netchine I; Rossignol S; Azzi S; Le Bouc Y Nestle Nutr Inst Workshop Ser; 2013; 71():65-73. PubMed ID: 23502140 [TBL] [Abstract][Full Text] [Related]
31. 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]
32. Renal abnormalities in beckwith-wiedemann syndrome are associated with 11p15.5 uniparental disomy. Goldman M; Smith A; Shuman C; Caluseriu O; Wei C; Steele L; Ray P; Sadowski P; Squire J; Weksberg R; Rosenblum ND J Am Soc Nephrol; 2002 Aug; 13(8):2077-84. PubMed ID: 12138139 [TBL] [Abstract][Full Text] [Related]
33. Imprinted anomalies in fetal and childhood growth disorders: the model of Russell-Silver and Beckwith-Wiedemann syndromes. Netchine I; Rossignol S; Azzi S; Brioude F; Le Bouc Y Endocr Dev; 2012; 23():60-70. PubMed ID: 23182821 [TBL] [Abstract][Full Text] [Related]
34. Paternal uniparental disomy 11p15.5 in the pancreatic nodule of an infant with Costello syndrome: Shared mechanism for hyperinsulinemic hypoglycemia in neonates with Costello and Beckwith-Wiedemann syndrome and somatic loss of heterozygosity in Costello syndrome driving clonal expansion. Gripp KW; Robbins KM; Sheffield BS; Lee AF; Patel MS; Yip S; Doyle D; Stabley D; Sol-Church K Am J Med Genet A; 2016 Mar; 170(3):559-64. PubMed ID: 26572961 [TBL] [Abstract][Full Text] [Related]
35. 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]
36. Association of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndrome. Smith AC; Squire JA; Thorner P; Zielenska M; Shuman C; Grant R; Chitayat D; Nishikawa JL; Weksberg R Pediatr Dev Pathol; 2001; 4(6):550-8. PubMed ID: 11826361 [TBL] [Abstract][Full Text] [Related]
37. Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5. Paulsen M; Davies KR; Bowden LM; Villar AJ; Franck O; Fuermann M; Dean WL; Moore TF; Rodrigues N; Davies KE; Hu RJ; Feinberg AP; Maher ER; Reik W; Walter J Hum Mol Genet; 1998 Jul; 7(7):1149-59. PubMed ID: 9618174 [TBL] [Abstract][Full Text] [Related]
38. A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5. Besnard-Guérin C; Newsham I; Winqvist R; Cavenee WK Hum Genet; 1996 Feb; 97(2):163-70. PubMed ID: 8566947 [TBL] [Abstract][Full Text] [Related]
39. [A peculiar form of neonatal adrenal insufficiency: the IMAGe association. Two new cases]. Ferey S; Merzoug V; Linglart A; Chaussain JL; Kalifa G J Radiol; 2003 Mar; 84(3):323-5. PubMed ID: 12736593 [TBL] [Abstract][Full Text] [Related]
40. Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences. Heide S; Chantot-Bastaraud S; Keren B; Harbison MD; Azzi S; Rossignol S; Michot C; Lackmy-Port Lys M; Demeer B; Heinrichs C; Newfield RS; Sarda P; Van Maldergem L; Trifard V; Giabicani E; Siffroi JP; Le Bouc Y; Netchine I; Brioude F J Med Genet; 2018 Mar; 55(3):205-213. PubMed ID: 29223973 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]