Journal of Genetic Medicine : eISSN 2383-8442 / pISSN 1226-1769

Fig. 1.

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Fig. 1. Imprinting at the H19/IGF2 (ICR1) locus and KCNQ1OT1/CDKN1C (ICR2) locus in the chromosomal region 11p15.5. Genetic and epigenetic disturbances in patients with Beckwith–Wiedemann syndrome and Silver–Russell syndrome.
Journal of Genetic Medicine 2021;18:24-30 https://doi.org/10.5734/JGM.2021.18.1.24
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