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Human Molecular Genetics
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October 11, 2017
A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability
Benjamin Davies, Laurence A Brown, Ondrej Cais, et al.
Human Molecular Genetics
|
January 28, 2014
Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis
Hilary C Martin, Grace E Kim, Alistair T Pagnamenta, et al.
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of 3
Search research articles
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Showing results (21-30 of 22) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 22 results.
Human Molecular Genetics
|
October 11, 2017
A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability
Benjamin Davies, Laurence A Brown, Ondrej Cais, et al.
Human Molecular Genetics
|
January 28, 2014
Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis
Hilary C Martin, Grace E Kim, Alistair T Pagnamenta, et al.
Page
of 3