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18 february 2019 18:01:17

 
De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairment (European Journal of Human Genetics)
 




 
61 viewsCategory: Genetics
 
Recombination within the Cepaea nemoralis supergene is confounded by incomplete penetrance and epistasis (Heredity)
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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