145 related articles for article (PubMed ID: 7802017)
21. Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome.
Kubota T; Saitoh S; Matsumoto T; Narahara K; Fukushima Y; Jinno Y; Niikawa N
Am J Med Genet; 1994 Feb; 49(4):378-83. PubMed ID: 7909196
[TBL] [Abstract][Full Text] [Related]
22. [Wiedemann-Beckwith syndrome: apropos of 20 cases].
Vacher C; Vazquez MP; Le Bouc Y; Schneid H
Rev Stomatol Chir Maxillofac; 1994; 95(2):192-3. PubMed ID: 8036428
[No Abstract] [Full Text] [Related]
23. No major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disorders.
Müller A; Soellner L; Binder G; Begemann M; Eggermann T
Am J Med Genet A; 2016 Jan; 170A(1):283-4. PubMed ID: 26447000
[No Abstract] [Full Text] [Related]
24. [Genomic imprinting and hereditary diseases].
Orstavik KH
Tidsskr Nor Laegeforen; 1999 Feb; 119(6):835-8. PubMed ID: 10101947
[TBL] [Abstract][Full Text] [Related]
25. CDKN1C expression in Beckwith-Wiedemann syndrome patients with allele imbalance.
Algar EM; Deeble GJ; Smith PJ
J Med Genet; 1999 Jul; 36(7):524-31. PubMed ID: 10424812
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. 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]
28. Monozygotic twinning and Wiedemann-Beckwith syndrome.
Clayton-Smith J; Read AP; Donnai D
Am J Med Genet; 1992 Feb; 42(4):633-7. PubMed ID: 1609846
[TBL] [Abstract][Full Text] [Related]
29. Beckwith-Wiedemann syndrome and the insulin-like growth factor-II gene. Does the genotype explain the phenotype?
Witte DP; Bove KE
Am J Pathol; 1994 Oct; 145(4):762-5. PubMed ID: 7943167
[No Abstract] [Full Text] [Related]
30. 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]
31. Genomic imprinting and cancer.
Tycko B
Results Probl Cell Differ; 1999; 25():133-69. PubMed ID: 10339745
[No Abstract] [Full Text] [Related]
32. 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]
33. 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]
34. Mom and pop genetics: genomic imprinting changes may illuminate cancer.
McBride G
J Natl Cancer Inst; 1997 Sep; 89(17):1256-8. PubMed ID: 9293913
[No Abstract] [Full Text] [Related]
35. Targeted regulation of imprinted genes by synthetic zinc-finger transcription factors.
Jouvenot Y; Ginjala V; Zhang L; Liu PQ; Oshimura M; Feinberg AP; Wolffe AP; Ohlsson R; Gregory PD
Gene Ther; 2003 Mar; 10(6):513-22. PubMed ID: 12621455
[TBL] [Abstract][Full Text] [Related]
36. [Wiedemann-Beckwith syndrome: clinical and epidemiological analysis of a consecutive series of cases in Spain].
Arroyo Carrera I; Martínez-Frías ML; Egüés Jimeno J; García Martínez MJ; Eloína Cimadevilla Sánchez C; Bermejo Sánchez E
An Esp Pediatr; 1999 Feb; 50(2):161-5. PubMed ID: 10199027
[TBL] [Abstract][Full Text] [Related]
37. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
[TBL] [Abstract][Full Text] [Related]
38. Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour.
Ogawa O; Eccles MR; Szeto J; McNoe LA; Yun K; Maw MA; Smith PJ; Reeve AE
Nature; 1993 Apr; 362(6422):749-51. PubMed ID: 8097018
[TBL] [Abstract][Full Text] [Related]
39. Beckwith-Wiedemann syndrome in a child with chromosome 18q deletion.
Brewer CM; Lam WW; Hayward C; Grace E; Maher ER; FitzPatrick DR
J Med Genet; 1998 Feb; 35(2):162-4. PubMed ID: 9507400
[TBL] [Abstract][Full Text] [Related]
40. Cloning of candidate genes involved in the Beckwith-Wiedemann syndrome and childhood tumors.
Alders M; Bliek J; Redeker B; Ryan A; Feinberg A; Westerveld A; Little P; Mannens M
Med Pediatr Oncol; 1996 Nov; 27(5):495-7. PubMed ID: 8827080
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
