191 related articles for article (PubMed ID: 15691772)
1. Intrauterine growth restriction--genetic causes and consequences.
Monk D; Moore GE
Semin Fetal Neonatal Med; 2004 Oct; 9(5):371-8. PubMed ID: 15691772
[TBL] [Abstract][Full Text] [Related]
2. (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]
3. 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]
4. Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth.
Jacob KJ; Robinson WP; Lefebvre L
Clin Genet; 2013 Oct; 84(4):326-34. PubMed ID: 23495910
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Epigenetics in Silver-Russell syndrome.
Rossignol S; Netchine I; Le Bouc Y; Gicquel C
Best Pract Res Clin Endocrinol Metab; 2008 Jun; 22(3):403-14. PubMed ID: 18538282
[TBL] [Abstract][Full Text] [Related]
7. No evidence for isolated imprinting mutations in the PEG1/MEST locus in Silver-Russell patients.
Schöherr N; Jäger S; Ranke MB; Wollmann HA; Binder G; Eggermann T
Eur J Med Genet; 2008; 51(4):322-4. PubMed ID: 18585117
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. The genetic aetiology of Silver-Russell syndrome.
Abu-Amero S; Monk D; Frost J; Preece M; Stanier P; Moore GE
J Med Genet; 2008 Apr; 45(4):193-9. PubMed ID: 18156438
[TBL] [Abstract][Full Text] [Related]
10. Hormonal regulation of fetal growth.
Gicquel C; Le Bouc Y
Horm Res; 2006; 65 Suppl 3():28-33. PubMed ID: 16612111
[TBL] [Abstract][Full Text] [Related]
11. Uniparental disomy: clinical indications for testing in growth retardation.
Eggermann T; Zerres K; Eggermann K; Moore G; Wollmann HA
Eur J Pediatr; 2002 Jun; 161(6):305-12. PubMed ID: 12029448
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Beckwith-Wiedemann syndrome.
Weksberg R; Shuman C; Smith AC
Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):12-23. PubMed ID: 16010676
[TBL] [Abstract][Full Text] [Related]
14. The role of imprinted genes in humans.
Ishida M; Moore GE
Mol Aspects Med; 2013; 34(4):826-40. PubMed ID: 22771538
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Silver-Russell syndrome and its genetic origins.
Rossignol S
J Endocrinol Invest; 2006; 29(1 Suppl):9-10. PubMed ID: 16615300
[TBL] [Abstract][Full Text] [Related]
17. Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome.
Eggermann T; Eggermann K; Schönherr N
Trends Genet; 2008 Apr; 24(4):195-204. PubMed ID: 18329128
[TBL] [Abstract][Full Text] [Related]
18. Is maternal duplication of 11p15 associated with Silver-Russell syndrome?
Eggermann T; Meyer E; Obermann C; Heil I; Schüler H; Ranke MB; Eggermann K; Wollmann HA
J Med Genet; 2005 May; 42(5):e26. PubMed ID: 15863658
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Myoclonus-dystonia due to maternal uniparental disomy.
Guettard E; Portnoi MF; Lohmann-Hedrich K; Keren B; Rossignol S; Winkler S; El Kamel I; Leu S; Apartis E; Vidailhet M; Klein C; Roze E
Arch Neurol; 2008 Oct; 65(10):1380-5. PubMed ID: 18852357
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
