Publication | Open Access
A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith–Wiedemann syndrome
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Citations
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References
2016
Year
Causes LossDevelopmental BiologyGenetic DisorderMedicineGeneticsEpigenetic ChangeFamilial Beckwith–wiedemann SyndromeAbnormal DevelopmentEpigenetic RegulationEpigeneticsMaternal Deletion Upstream
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