Weksberg R - Search Results

1

Advances in overgrowth syndromes: clinical classification to molecular delineation in Sotos syndrome and Beckwith-Wiedemann syndrome.

Cytrynbaum CS, Smith AC, Rubin T, Weksberg R. Cytrynbaum CS, et al. Among authors: weksberg r. Curr Opin Pediatr. 2005 Dec;17(6):740-6. doi: 10.1097/01.mop.0000187191.74295.97. Curr Opin Pediatr. 2005. PMID: 16282780 Review.

2

Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS region.

Weksberg R, Glaves M, Teshima I, Waziri M, Patil S, Williams BR. Weksberg R, et al. Genomics. 1990 Dec;8(4):693-8. doi: 10.1016/0888-7543(90)90256-t. Genomics. 1990. PMID: 2276740

3

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome.

Weksberg R, Shen DR, Fei YL, Song QL, Squire J. Weksberg R, et al. Nat Genet. 1993 Oct;5(2):143-50. doi: 10.1038/ng1093-143. Nat Genet. 1993. PMID: 8252039

4

Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted.

Weksberg R, Teshima I, Williams BR, Greenberg CR, Pueschel SM, Chernos JE, Fowlow SB, Hoyme E, Anderson IJ, Whiteman DA, et al. Weksberg R, et al. Hum Mol Genet. 1993 May;2(5):549-56. doi: 10.1093/hmg/2.5.549. Hum Mol Genet. 1993. PMID: 8518793

5

Molecular biology of Beckwith-Wiedemann syndrome.

Weksberg R, Squire JA. Weksberg R, et al. Med Pediatr Oncol. 1996 Nov;27(5):462-9. doi: 10.1002/(SICI)1096-911X(199611)27:5<462::AID-MPO13>3.0.CO;2-C. Med Pediatr Oncol. 1996. PMID: 8827075 Review.

6

Molecular genetics of Beckwith-Wiedemann syndrome.

Li M, Squire JA, Weksberg R. Li M, et al. Among authors: weksberg r. Curr Opin Pediatr. 1997 Dec;9(6):623-9. doi: 10.1097/00008480-199712000-00012. Curr Opin Pediatr. 1997. PMID: 9425596 Review.

7

Overgrowth syndromes and genomic imprinting: from mouse to man.

Li M, Squire JA, Weksberg R. Li M, et al. Among authors: weksberg r. Clin Genet. 1998 Mar;53(3):165-70. Clin Genet. 1998. PMID: 9630066 Review.

8

Molecular genetics of Wiedemann-Beckwith syndrome.

Li M, Squire JA, Weksberg R. Li M, et al. Among authors: weksberg r. Am J Med Genet. 1998 Oct 2;79(4):253-9. Am J Med Genet. 1998. PMID: 9781904 Review.

9

Decreased elastin deposition and high proliferation of fibroblasts from Costello syndrome are related to functional deficiency in the 67-kD elastin-binding protein.

Hinek A, Smith AC, Cutiongco EM, Callahan JW, Gripp KW, Weksberg R. Hinek A, et al. Among authors: weksberg r. Am J Hum Genet. 2000 Mar;66(3):859-72. doi: 10.1086/302829. Am J Hum Genet. 2000. PMID: 10712202 Free PMC article.

10

Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome.

Squire JA, Li M, Perlikowski S, Fei YL, Bayani J, Zhang ZM, Weksberg R. Squire JA, et al. Among authors: weksberg r. Genomics. 2000 May 1;65(3):234-42. doi: 10.1006/geno.2000.6155. Genomics. 2000. PMID: 10857747

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