Genetics
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18 february 2019 18:01:17 |
| Disruption of KCNQ1 prevents methylation of the ICR2 and supports the hypothesis that its transcription is necessary for imprint establishment (European Journal of Human Genetics) |
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 De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairment (European Journal of Human Genetics)A pilot eConsultation service in Eastern Ontario: bridging clinical genetics and primary care (European Journal of Human Genetics) 
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