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.
180 related articles for article (PubMed ID: 24767654)
1. Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer. Chen CP; Su YN; Chen SU; Chang TY; Wu PC; Chern SR; Wu PS; Kuo YL; Wang W Taiwan J Obstet Gynecol; 2014 Mar; 53(1):90-4. PubMed ID: 24767654 [TBL] [Abstract][Full Text] [Related]
2. Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndrome. Chen CP; Chern SR; Lin CH; Hsu CY; Lin HY; Wu FT; Chen SW; Wang W Taiwan J Obstet Gynecol; 2021 Nov; 60(6):1103-1106. PubMed ID: 34794746 [TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of paternal duplication of 11p15.5→14.3: Its implication of Beckwith-Wiedemann syndrome. Chen KJ; Liu YM; Li CH; Chang YL; Chang SD Taiwan J Obstet Gynecol; 2016 Dec; 55(6):877-880. PubMed ID: 28040139 [TBL] [Abstract][Full Text] [Related]
4. Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia. Chen CP; Su YN; Lin MH; Wang TY; Chern SR; Kuo YL; Chen YT; Wang W Taiwan J Obstet Gynecol; 2014 Mar; 53(1):68-73. PubMed ID: 24767650 [TBL] [Abstract][Full Text] [Related]
5. Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies. Lim D; Bowdin SC; Tee L; Kirby GA; Blair E; Fryer A; Lam W; Oley C; Cole T; Brueton LA; Reik W; Macdonald F; Maher ER Hum Reprod; 2009 Mar; 24(3):741-7. PubMed ID: 19073614 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Beckwith-Weidemann syndrome with IC2 (KvDMR1) hypomethylation defect: a novel mutation. Pandita A; Gupta S; Gupta G; Panghal A BMJ Case Rep; 2018 Mar; 2018():. PubMed ID: 29602885 [TBL] [Abstract][Full Text] [Related]
8. Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome. Diaz-Meyer N; Day CD; Khatod K; Maher ER; Cooper W; Reik W; Junien C; Graham G; Algar E; Der Kaloustian VM; Higgins MJ J Med Genet; 2003 Nov; 40(11):797-801. PubMed ID: 14627666 [TBL] [Abstract][Full Text] [Related]
9. The heterogeneity of hyperinsulinaemic hypoglycaemia in 19 patients with Beckwith-Wiedemann syndrome due to KvDMR1 hypomethylation. Senniappan S; Ismail D; Shipster C; Beesley C; Hussain K J Pediatr Endocrinol Metab; 2015 Jan; 28(1-2):83-6. PubMed ID: 24468603 [TBL] [Abstract][Full Text] [Related]
11. Overrepresentation of pregnancies conceived by artificial reproductive technology in prenatally identified fetuses with Beckwith-Wiedemann syndrome. Johnson JP; Beischel L; Schwanke C; Styren K; Crunk A; Schoof J; Elias AF J Assist Reprod Genet; 2018 Jun; 35(6):985-992. PubMed ID: 29936652 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Pregnancy outcomes after assisted human reproduction. Okun N; Sierra S; ; J Obstet Gynaecol Can; 2014 Jan; 36(1):64-83. PubMed ID: 24444289 [TBL] [Abstract][Full Text] [Related]
14. Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes. Sperandeo MP; Ungaro P; Vernucci M; Pedone PV; Cerrato F; Perone L; Casola S; Cubellis MV; Bruni CB; Andria G; Sebastio G; Riccio A Am J Hum Genet; 2000 Mar; 66(3):841-7. PubMed ID: 10712200 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Giant omphalocele and "prune belly" sequence as components of the Beckwith-Wiedemann syndrome. Sinico M; Touboul C; Haddad B; Encha-Razavi F; Paniel JB; Gicquel C; Gérard-Blanluet M Am J Med Genet A; 2004 Aug; 129A(2):198-200. PubMed ID: 15316976 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Mosaic genome-wide paternal uniparental disomy after discordant results from primary fetal samples and cultured cells. Mastromoro G; Guadagnolo D; Marchionni E; Torres B; Goldoni M; Onori A; Bernardini L; De Luca A; Torrente I; Pizzuti A Am J Med Genet A; 2023 Apr; 191(4):1101-1106. PubMed ID: 36598152 [TBL] [Abstract][Full Text] [Related]
19. Methylation analysis of KvDMR1 in human oocytes. Geuns E; Hilven P; Van Steirteghem A; Liebaers I; De Rycke M J Med Genet; 2007 Feb; 44(2):144-7. PubMed ID: 16950814 [TBL] [Abstract][Full Text] [Related]
20. Different methylation patterns in BWS/SRS cases clarified by MS-MLPA. Lukova M; Todorova A; Todorov T; Mitev V Mol Biol Rep; 2013 Jan; 40(1):263-8. PubMed ID: 23086270 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]