Publication | Closed Access
IGF2 is parentally imprinted during human embryogenesis and in the Beckwith–Wiedemann syndrome
296
Citations
14
References
1993
Year
Developmental BiologyTissue DevelopmentGeneticsMorphogenesisHuman EmbryogenesisBeckwith–wiedemann SyndromeHuman Embryonic DevelopmentEmbryonic DevelopmentAbnormal DevelopmentMedicineCell BiologyEpigeneticsCell DevelopmentEmbryologyReproductive Endocrinology
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