Imprinting mutations in the Beckwith—Wiedemann syndrome suggested by an altered imprinting pattern in the <i>IGF2–H19</i> domain
Wolf Reik(Altos Labs), Eamonn R. Maher(University of Birmingham), Yves Le Bouc(Inserm), H Schneid(Hôpital d'Enfants), Wendy A. Bickmore(University of Edinburgh), Keith Brown(University of Bristol)
Cited by 215
Related Papers
A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction
|Nature|1998|2.4k
Child Health, Developmental Plasticity, and Epigenetic Programming
|Endocrine Reviews|2010|625
Chromatin decondensation and nuclear reorganization of the <i>HoxB</i> locus upon induction of transcription
|Genes & Development|2004|625
Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement
|Nature Reviews Endocrinology|2018|596