University of Montpellier-ko ikertzaileekin lankidetzan egindako argitalpenak (1)

2013

  1. Simultaneous hyper- and hypomethylation at imprinted loci in a subset of patients with gnas epimutations underlies a complex and different mechanism of multilocus methylation defect in pseudohypoparathyroidism type 1b

    Human Mutation, Vol. 34, Núm. 8, pp. 1172-1180