218 related articles for article (PubMed ID: 27165005)
21. Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders.
Fontana L; Bedeschi MF; Maitz S; Cereda A; Faré C; Motta S; Seresini A; D'Ursi P; Orro A; Pecile V; Calvello M; Selicorni A; Lalatta F; Milani D; Sirchia SM; Miozzo M; Tabano S
Epigenetics; 2018; 13(9):897-909. PubMed ID: 30221575
[TBL] [Abstract][Full Text] [Related]
22. Epigenetic and genetic mechanisms of abnormal 11p15 genomic imprinting in Silver-Russell and Beckwith-Wiedemann syndromes.
Demars J; Le Bouc Y; El-Osta A; Gicquel C
Curr Med Chem; 2011; 18(12):1740-50. PubMed ID: 21466477
[TBL] [Abstract][Full Text] [Related]
23. Beckwith Wiedemann imprinting defect found in leucocyte but not buccal DNA in a child born small for gestational age.
Murphy R; Mackay D; Mitchell EA
BMC Med Genet; 2012 Nov; 13():99. PubMed ID: 23116464
[TBL] [Abstract][Full Text] [Related]
24. The Frequency of Methylation Abnormalities Among Estonian Patients Selected by Clinical Diagnostic Scoring Systems for Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome.
Vals MA; Yakoreva M; Kahre T; Mee P; Muru K; Joost K; Teek R; Soellner L; Eggermann T; Õunap K
Genet Test Mol Biomarkers; 2015 Dec; 19(12):684-91. PubMed ID: 26505556
[TBL] [Abstract][Full Text] [Related]
25. Imprinted disorders and growth.
Giabicani É; Brioude F; Le Bouc Y; Netchine I
Ann Endocrinol (Paris); 2017 Jun; 78(2):112-113. PubMed ID: 28478949
[TBL] [Abstract][Full Text] [Related]
26. Allele-specific methylated multiplex real-time quantitative PCR (ASMM RTQ-PCR), a powerful method for diagnosing loss of imprinting of the 11p15 region in Russell Silver and Beckwith Wiedemann syndromes.
Azzi S; Steunou V; Rousseau A; Rossignol S; Thibaud N; Danton F; Le Jule M; Gicquel C; Le Bouc Y; Netchine I
Hum Mutat; 2011 Feb; 32(2):249-58. PubMed ID: 21280150
[TBL] [Abstract][Full Text] [Related]
27. Silver-Russell and Beckwith-Wiedemann syndromes: opposite (epi)mutations in 11p15 result in opposite clinical pictures.
Eggermann T
Horm Res; 2009 Apr; 71 Suppl 2():30-5. PubMed ID: 19407494
[TBL] [Abstract][Full Text] [Related]
28. Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients.
Rovina D; La Vecchia M; Cortesi A; Fontana L; Pesant M; Maitz S; Tabano S; Bodega B; Miozzo M; Sirchia SM
Sci Rep; 2020 May; 10(1):8275. PubMed ID: 32427849
[TBL] [Abstract][Full Text] [Related]
29. Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell Syndrome.
Pignata L; Sparago A; Palumbo O; Andreucci E; Lapi E; Tenconi R; Carella M; Riccio A; Cerrato F
Genes (Basel); 2021 Apr; 12(4):. PubMed ID: 33923683
[TBL] [Abstract][Full Text] [Related]
30. Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domains.
Eggermann T; Begemann M; Pfeiffer L
Clin Epigenetics; 2021 Feb; 13(1):30. PubMed ID: 33541417
[TBL] [Abstract][Full Text] [Related]
31. MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment.
Priolo M; Sparago A; Mammì C; Cerrato F; Laganà C; Riccio A
Eur J Hum Genet; 2008 May; 16(5):565-71. PubMed ID: 18212817
[TBL] [Abstract][Full Text] [Related]
32. High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith-Wiedemann syndrome.
Baskin B; Choufani S; Chen YA; Shuman C; Parkinson N; Lemyre E; Micheil Innes A; Stavropoulos DJ; Ray PN; Weksberg R
Hum Genet; 2014 Mar; 133(3):321-30. PubMed ID: 24154661
[TBL] [Abstract][Full Text] [Related]
33. Prenatal correction of IGF2 to rescue the growth phenotypes in mouse models of Beckwith-Wiedemann and Silver-Russell syndromes.
Liao J; Zeng TB; Pierce N; Tran DA; Singh P; Mann JR; Szabó PE
Cell Rep; 2021 Feb; 34(6):108729. PubMed ID: 33567274
[TBL] [Abstract][Full Text] [Related]
34. Feasibility study on the use of methylation-specific MLPA for the 11p15 region on prenatal samples.
Gede LB; Hahnemann JM; Tümer Z; Brøndum-Nielsen K; Grønskov K
Prenat Diagn; 2016 Jan; 36(1):100-3. PubMed ID: 26590364
[No Abstract] [Full Text] [Related]
35. A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver-Russell syndrome phenotype.
Mio C; Allegri L; Passon N; Bregant E; Demori E; Franzoni A; Driul D; Riccio A; Damante G; Baldan F
Eur J Hum Genet; 2021 Mar; 29(3):447-454. PubMed ID: 33177595
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders.
Soejima H; Higashimoto K
J Hum Genet; 2013 Jul; 58(7):402-9. PubMed ID: 23719190
[TBL] [Abstract][Full Text] [Related]
38. The centromeric 11p15 imprinting centre is also involved in Silver-Russell syndrome.
Schönherr N; Meyer E; Roos A; Schmidt A; Wollmann HA; Eggermann T
J Med Genet; 2007 Jan; 44(1):59-63. PubMed ID: 16963484
[TBL] [Abstract][Full Text] [Related]
39. (Epi)mutations in 11p15 significantly contribute to Silver-Russell syndrome: but are they generally involved in growth retardation?
Schönherr N; Meyer E; Eggermann K; Ranke MB; Wollmann HA; Eggermann T
Eur J Med Genet; 2006; 49(5):414-8. PubMed ID: 16603426
[TBL] [Abstract][Full Text] [Related]
40. First-time application of droplet digital PCR for methylation testing of the 11p15.5 imprinting regions.
Schlaich E; Hubens WHG; Eggermann T
Mol Genet Genomic Med; 2023 Dec; 11(12):e2264. PubMed ID: 37519217
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
