165 related articles for article (PubMed ID: 18571544)
1. Epigenotype, phenotype, and tumors in patients with isolated hemihyperplasia.
Bliek J; Maas S; Alders M; Merks JH; Mannens M
J Pediatr; 2008 Jul; 153(1):95-100. PubMed ID: 18571544
[TBL] [Abstract][Full Text] [Related]
2. Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome.
Cooper WN; Luharia A; Evans GA; Raza H; Haire AC; Grundy R; Bowdin SC; Riccio A; Sebastio G; Bliek J; Schofield PN; Reik W; Macdonald F; Maher ER
Eur J Hum Genet; 2005 Sep; 13(9):1025-32. PubMed ID: 15999116
[TBL] [Abstract][Full Text] [Related]
3. [Uniparental disomy of chromosome 11 in a patient with Beckwith-Wiedemann syndrome. First reported case in Iceland].
Pálsson GI; Finnsdóttir V; Jóhannsson JH; Ingvarsson S
Laeknabladid; 2005 Nov; 91(11):837-40. PubMed ID: 16264244
[TBL] [Abstract][Full Text] [Related]
4. Mitotic recombination and uniparental disomy in Beckwith-Wiedemann syndrome.
Cooper WN; Curley R; Macdonald F; Maher ER
Genomics; 2007 May; 89(5):613-7. PubMed ID: 17337339
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologies.
Shuman C; Smith AC; Steele L; Ray PN; Clericuzio C; Zackai E; Parisi MA; Meadows AT; Kelly T; Tichauer D; Squire JA; Sadowski P; Weksberg R
Am J Med Genet A; 2006 Jul; 140(14):1497-503. PubMed ID: 16770802
[TBL] [Abstract][Full Text] [Related]
7. Proportion of cells with paternal 11p15 uniparental disomy correlates with organ enlargement in Wiedemann-beckwith syndrome.
Itoh N; Becroft DM; Reeve AE; Morison IM
Am J Med Genet; 2000 May; 92(2):111-6. PubMed ID: 10797434
[TBL] [Abstract][Full Text] [Related]
8. Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS.
Bliek J; Maas SM; Ruijter JM; Hennekam RC; Alders M; Westerveld A; Mannens MM
Hum Mol Genet; 2001 Mar; 10(5):467-76. PubMed ID: 11181570
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Uniparental paternal disomy in a genetic cancer-predisposing syndrome.
Henry I; Bonaiti-Pellié C; Chehensse V; Beldjord C; Schwartz C; Utermann G; Junien C
Nature; 1991 Jun; 351(6328):665-7. PubMed ID: 1675767
[TBL] [Abstract][Full Text] [Related]
12. LIT1 and H19 methylation defects in isolated hemihyperplasia.
Martin RA; Grange DK; Zehnbauer B; Debaun MR
Am J Med Genet A; 2005 Apr; 134A(2):129-31. PubMed ID: 15651076
[TBL] [Abstract][Full Text] [Related]
13. SNP arrays in Beckwith-Wiedemann syndrome: an improved diagnostic strategy.
Keren B; Chantot-Bastaraud S; Brioude F; Mach C; Fonteneau E; Azzi S; Depienne C; Brice A; Netchine I; Le Bouc Y; Siffroi JP; Rossignol S
Eur J Med Genet; 2013 Oct; 56(10):546-50. PubMed ID: 23892181
[TBL] [Abstract][Full Text] [Related]
14. Epigenotype and phenotype correlations in patients with Beckwith-Wiedemann syndrome.
Bilgin B; Kabaçam S; Taşkıran E; Şimşek-Kiper PÖ; Alanay Y; Boduroğlu K; Utine GE
Turk J Pediatr; 2018; 60(5):506-513. PubMed ID: 30968633
[TBL] [Abstract][Full Text] [Related]
15. Broad clinical spectrum in Silver-Russell syndrome and consequences for genetic testing in growth retardation.
Eggermann T; Gonzalez D; Spengler S; Arslan-Kirchner M; Binder G; Schönherr N
Pediatrics; 2009 May; 123(5):e929-31. PubMed ID: 19364767
[TBL] [Abstract][Full Text] [Related]
16. Methylation analysis in tongue tissue of BWS patients identifies the (EPI)genetic cause in 3 patients with normal methylation levels in blood.
Alders M; Maas SM; Kadouch DJ; van der Lip K; Bliek J; van der Horst CM; Mannens MM
Eur J Med Genet; 2014; 57(6):293-7. PubMed ID: 24704790
[TBL] [Abstract][Full Text] [Related]
17. Diagnostic criteria and tumor screening for individuals with isolated hemihyperplasia.
Clericuzio CL; Martin RA
Genet Med; 2009 Mar; 11(3):220-2. PubMed ID: 19367194
[TBL] [Abstract][Full Text] [Related]
18. Constitutional mosaic genome-wide uniparental disomy due to diploidisation: an unusual cancer-predisposing mechanism.
Romanelli V; Nevado J; Fraga M; Trujillo AM; Mori MÁ; Fernández L; Pérez de Nanclares G; Martínez-Glez V; Pita G; Meneses H; Gracia R; García-Miñaur S; García de Miguel P; Lecumberri B; Rodríguez JI; González Neira A; Monk D; Lapunzina P
J Med Genet; 2011 Mar; 48(3):212-6. PubMed ID: 21097775
[TBL] [Abstract][Full Text] [Related]
19. Epigenetic deregulation of imprinting in congenital diseases of aberrant growth.
Delaval K; Wagschal A; Feil R
Bioessays; 2006 May; 28(5):453-9. PubMed ID: 16615080
[TBL] [Abstract][Full Text] [Related]
20. Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS).
Bliek J; Gicquel C; Maas S; Gaston V; Le Bouc Y; Mannens M
J Pediatr; 2004 Dec; 145(6):796-9. PubMed ID: 15580204
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]