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Results: 12

Related Articles by Review for PubMed (Select 9520460)

1.

Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples.

Schwienbacher C, Sabbioni S, Campi M, Veronese A, Bernardi G, Menegatti A, Hatada I, Mukai T, Ohashi H, Barbanti-Brodano G, Croce CM, Negrini M.

Proc Natl Acad Sci U S A. 1998 Mar 31;95(7):3873-8.

2.

Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors.

Mannens M, Alders M, Redeker B, Bliek J, Steenman M, Wiesmeyer C, de Meulemeester M, Ryan A, Kalikin L, Voƻte T, De Kraker J, Hoovers J, Slater R, Feinberg A, Little P, Westerveld A.

Med Pediatr Oncol. 1996 Nov;27(5):490-4. Review.

PMID:
8827079
3.

Multiple genetic abnormalities of 11p15 in Wilms' tumor.

Feinberg AP.

Med Pediatr Oncol. 1996 Nov;27(5):484-9. Review.

PMID:
8827078
4.

Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways.

Steenman M, Westerveld A, Mannens M.

Genes Chromosomes Cancer. 2000 May;28(1):1-13. Review.

PMID:
10738297
5.

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. doi: 10.1159/000192433. Epub 2009 Apr 29. Review.

PMID:
19407494
6.

Molecular genetics of Beckwith-Wiedemann syndrome.

Li M, Squire JA, Weksberg R.

Curr Opin Pediatr. 1997 Dec;9(6):623-9. Review.

PMID:
9425596
7.

Genomic imprinting and Beckwith-Wiedemann syndrome.

Hatada I, Mukai T.

Histol Histopathol. 2000 Jan;15(1):309-12. Review.

PMID:
10668219
8.

Beckwith-Wiedemann syndrome.

Choufani S, Shuman C, Weksberg R.

Am J Med Genet C Semin Med Genet. 2010 Aug 15;154C(3):343-54. doi: 10.1002/ajmg.c.30267. Review.

PMID:
20803657
9.

Beck-Wiedemann syndrome and Wilms' tumour.

Ward A.

Mol Hum Reprod. 1997 Feb;3(2):157-68. Review.

10.

Paternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome. A new case and review of the literature.

Brown KW, Gardner A, Williams JC, Mott MG, McDermott A, Maitland NJ.

Cancer Genet Cytogenet. 1992 Jan;58(1):66-70. Review.

PMID:
1728953
11.

Molecular biology of Beckwith-Wiedemann syndrome.

Weksberg R, Squire JA.

Med Pediatr Oncol. 1996 Nov;27(5):462-9. Review.

PMID:
8827075
12.

Transcriptional derepression as a cause of genetic diseases.

Gabellini D, Tupler R, Green MR.

Curr Opin Genet Dev. 2003 Jun;13(3):239-45. Review.

PMID:
12787785
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