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Science Immunology
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December 15, 2019
Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in <i>STAT2</i>
Christopher J A Duncan, Benjamin J Thompson, Rui Chen, et al.
Nature Genetics
|
July 31, 2007
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy
Anna Richards, Arn M J M van den Maagdenberg, Joanna C Jen, et al.
Nature Genetics
|
November 22, 2016
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Christian R Marshall, Daniel P Howrigan, Daniele Merico, et al.
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Showing results (191-200 of 193) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 193 results.
Science Immunology
|
December 15, 2019
Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in <i>STAT2</i>
Christopher J A Duncan, Benjamin J Thompson, Rui Chen, et al.
Nature Genetics
|
July 31, 2007
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy
Anna Richards, Arn M J M van den Maagdenberg, Joanna C Jen, et al.
Nature Genetics
|
November 22, 2016
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Christian R Marshall, Daniel P Howrigan, Daniele Merico, et al.
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of 20