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Year Number of Results
2002 3
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2005 5
2006 3
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2008 3
2011 1
2019 1
2024 0

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Page 1
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. Cooper WN, et al. Among authors: sebastio g. Eur J Hum Genet. 2005 Sep;13(9):1025-32. doi: 10.1038/sj.ejhg.5201463. Eur J Hum Genet. 2005. PMID: 15999116
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour.
Cerrato F, Sparago A, Verde G, De Crescenzo A, Citro V, Cubellis MV, Rinaldi MM, Boccuto L, Neri G, Magnani C, D'Angelo P, Collini P, Perotti D, Sebastio G, Maher ER, Riccio A. Cerrato F, et al. Among authors: sebastio g. Hum Mol Genet. 2008 May 15;17(10):1427-35. doi: 10.1093/hmg/ddn031. Epub 2008 Feb 1. Hum Mol Genet. 2008. PMID: 18245780 Free article.
Trisomy 18 and hypertrophy cardiomyopathy in an 18-year-old woman.
Limongelli G, Pacileo G, Melis D, Calabro' P, Digilio MC, Sarkozy A, Maddaloni V, Capozzi G, Sebastio G, Andria G, Calabro' R. Limongelli G, et al. Among authors: sebastio g. Am J Med Genet A. 2008 Feb 1;146A(3):327-9. doi: 10.1002/ajmg.a.32149. Am J Med Genet A. 2008. PMID: 18203191 No abstract available.
23 results