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The Lancet. Neurology
|
December 3, 2013
The genetic basis of DOORS syndrome: an exome-sequencing study
Philippe M Campeau, Dalia Kasperaviciute, James T Lu, et al.
Nature Genetics
|
September 25, 2012
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature
Gillian I Rice, Paul R Kasher, Gabriella M A Forte, et al.
Nature Genetics
|
January 24, 2012
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus
Beverley H Anderson, Paul R Kasher, Josephine Mayer, et al.
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Search research articles
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Showing results (11-20 of 13) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 13 results.
The Lancet. Neurology
|
December 3, 2013
The genetic basis of DOORS syndrome: an exome-sequencing study
Philippe M Campeau, Dalia Kasperaviciute, James T Lu, et al.
Nature Genetics
|
September 25, 2012
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature
Gillian I Rice, Paul R Kasher, Gabriella M A Forte, et al.
Nature Genetics
|
January 24, 2012
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus
Beverley H Anderson, Paul R Kasher, Josephine Mayer, et al.
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of 2