Publication | Closed Access

De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch

Developmental BiologyGeneticsMaternal Imprint SwitchMouse Embryos ResultMolecular GeneticsGerm Cell DevelopmentHuman Embryonic DevelopmentReproductive BiologyEarly HumanEmbryonic DevelopmentMedicineEpigeneticsEmbryologyHuman Reproduction