Sequence and functional comparison in the Beckwith–Wiedemann region: implications for a novel imprinting centre and extended imprinting

By Engemann Sabine  

Human Molecular Genetics, Vol. 9, Iss. 18, 2000-11 ,pp. : 2691-2706

Oxford University Press

Access to resources Recommend Favorite

Different mechanisms cause imprinting defects at the IGF2 / H19 locus in BeckwithWiedemann syndrome and Wilms' tumour

By Cerrato Flavia   Sparago Angela   Verde Gaetano   De Crescenzo Agostina   Citro Valentina   Cubellis Maria Vittoria   Rinaldi Maria Michela   Boccuto Luigi   Neri Giovanni   Magnani Cinzia   D'Angelo Paolo   Collini Paola   Perotti Daniela   Sebastio Gianfranco   Maher Eamonn R.   Riccio Andrea  

Human Molecular Genetics, Vol. 17, Iss. 10, 2008-05 ,pp. : 1427-1435

Oxford University Press

Access to resources Recommend Favorite

Imprinting of IGF2 and H19 : Lack of Reciprocity in Sporadic Beckwith-Wiedemann Syndrome

By Joyce Johanna A.   Lam Wayne K.  

Human Molecular Genetics, Vol. 6, Iss. 9, 1997-01 ,pp. : 1543-1548

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite