Sequence conservation and variability of imprinting in the Beckwith–Wiedemann syndrome gene cluster in human and mouse

By Paulsen Martina  

Human Molecular Genetics, Vol. 9, Iss. 12, 2000-07 ,pp. : 1829-1841

Oxford University Press

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Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith–Wiedemann syndrome and Silver–Russell syndrome

By Nativio Raffaella   Sparago Angela   Ito Yoko   Weksberg Rosanna   Riccio Andrea   Murrell Adele  

Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1363-1374

Oxford University Press

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Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith–Wiedemann syndrome region in chromosome 11p15.5

By Davies K.E.  

Human Molecular Genetics, Vol. 7, Iss. 7, 1998-07 ,pp. : 1149-1159

Oxford University Press

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An association between variants in the IGF2 gene and Beckwith–Wiedemann syndrome: interaction between genotype and epigenotype

By Murrell Adele  

Human Molecular Genetics, Vol. 13, Iss. 2, 2004-01 ,pp. : 247-255

Oxford University Press

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Imprinting Mutation in the Beckwith-Wiedemann Syndrome Leads to Biallelic IGF2 expression through an H19 -Independent Pathway

By Brown Keith W.   Villar Angela J.   Bickmore Wendy   Clayton-Smith Jill   Catchpoole Daniel   Maher Eamonn R.   Reik Wolf  

Human Molecular Genetics, Vol. 5, Iss. 12, 1996-12 ,pp. : 2027-2032

Oxford University Press

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