151 related articles for article (PubMed ID: 8036428)
21. Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor.
Prawitt D; Enklaar T; Gärtner-Rupprecht B; Spangenberg C; Lausch E; Reutzel D; Fees S; Korzon M; Brozek I; Limon J; Housman DE; Pelletier J; Zabel B
Nat Genet; 2005 Aug; 37(8):785-6; author reply 786-7. PubMed ID: 16049499
[No Abstract] [Full Text] [Related]
22. p57KIP2 targeted disruption and Beckwith-Wiedemann syndrome: is the inhibitor just a contributor?
Swanger WJ; Roberts JM
Bioessays; 1997 Oct; 19(10):839-42. PubMed ID: 9363677
[TBL] [Abstract][Full Text] [Related]
23. Surgical correction of macroglossia in Beckwith-Wiedemann syndrome.
Sokoloski PM; Ogle RG; Waite DE
J Oral Surg; 1978 Mar; 36(3):212-5. PubMed ID: 272454
[TBL] [Abstract][Full Text] [Related]
24. Beckwith-Wiedemann syndrome.
Norman AM; Read AP; Donnai D
J Med Genet; 1992 Sep; 29(9):679. PubMed ID: 1404305
[No Abstract] [Full Text] [Related]
25. Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome.
Weksberg R; Shen DR; Fei YL; Song QL; Squire J
Nat Genet; 1993 Oct; 5(2):143-50. PubMed ID: 8252039
[TBL] [Abstract][Full Text] [Related]
26. IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome.
Ohlsson R; Nyström A; Pfeifer-Ohlsson S; Töhönen V; Hedborg F; Schofield P; Flam F; Ekström TJ
Nat Genet; 1993 May; 4(1):94-7. PubMed ID: 8513333
[TBL] [Abstract][Full Text] [Related]
27. [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]
28. Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome.
Schneid H; Seurin D; Vazquez MP; Gourmelen M; Cabrol S; Le Bouc Y
J Med Genet; 1993 May; 30(5):353-62. PubMed ID: 8320696
[TBL] [Abstract][Full Text] [Related]
29. Treatment of macroglossia in a child with Beckwith-Wiedemann syndrome.
Dios PD; Posse JL; Sanromán JF; García EV
J Oral Maxillofac Surg; 2000 Sep; 58(9):1058-61. PubMed ID: 10981990
[No Abstract] [Full Text] [Related]
30. Molecular biology of Beckwith-Wiedemann syndrome.
Weksberg R; Squire JA
Med Pediatr Oncol; 1996 Nov; 27(5):462-9. PubMed ID: 8827075
[TBL] [Abstract][Full Text] [Related]
31. "Double-muscle" trait in cattle: a possible model for Wiedemann-Beckwith syndrome.
Best LG; Gilbert-Barness E; Gerrard DE; Gendron-Fitzpatrick A; Opitz JM
Fetal Pediatr Pathol; 2006; 25(1):9-20. PubMed ID: 16754485
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. A child with Beckwith-Wiedemann syndrome and posterior urethral valves.
Buyukcelik M; Satar N; Dursun H; Bayazit Y; Bayazit AK; Soran M; Noyan A; Anarat A
Genet Couns; 2005; 16(1):41-4. PubMed ID: 15844777
[TBL] [Abstract][Full Text] [Related]
34. Absence of detectable chromosomal and molecular abnormalities in monozygotic twins discordant for the Wiedemann-Beckwith syndrome.
Litz CE; Taylor KA; Qiu JS; Pescovitz OH; de Martinville B
Am J Med Genet; 1988 Jul; 30(3):821-33. PubMed ID: 3189402
[TBL] [Abstract][Full Text] [Related]
35. Beckwith-Wiedemann syndrome: dental management.
Garvey MT; Daly D; McNamara T
Int J Paediatr Dent; 1997 Jun; 7(2):95-9. PubMed ID: 9524461
[TBL] [Abstract][Full Text] [Related]
36. Surgical treatment of macroglossia in patients with Beckwith-Wiedemann syndrome: a 20-year experience and review of the literature.
Kadouch DJ; Maas SM; Dubois L; van der Horst CM
Int J Oral Maxillofac Surg; 2012 Mar; 41(3):300-8. PubMed ID: 22104000
[TBL] [Abstract][Full Text] [Related]
37. Chest wall hamartoma with Wiedemann-Beckwith syndrome: clinical report and brief review of chromosome 11p15.5-related tumors.
Jonas RE; Kimonis VE
Am J Med Genet; 2001 Jul; 101(3):221-5. PubMed ID: 11424137
[TBL] [Abstract][Full Text] [Related]
38. [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]
39. Treatment of the craniofacial complications of Beckwith-Wiedemann syndrome.
Menard RM; Delaire J; Schendel SA
Plast Reconstr Surg; 1995 Jul; 96(1):27-33. PubMed ID: 7604127
[TBL] [Abstract][Full Text] [Related]
40. Nonimmune fetal hydrops and placentomegaly: diagnosis of familial Wiedemann-Beckwith syndrome with trisomy 11p15 using FISH.
Drut RM; Drut R
Am J Med Genet; 1996 Mar; 62(2):145-9. PubMed ID: 8882394
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
