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Human Genetics
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February 6, 2010
Novel human pathological mutations. Gene symbol: SCN1A. Disease: Myoclonic epilepsy of infancy
F E Rocca, E V De Marco, F Annesi, et al.
Human Genetics
|
April 21, 2011
Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson disease
P Tarantino, F Annesi, V Scornaienchi, et al.
BMC Bioinformatics
|
April 29, 2019
DNAscan: personal computer compatible NGS analysis, annotation and visualisation
A Iacoangeli, A Al Khleifat, W Sproviero, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 21, 2010
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis
F L Conforti, W Sproviero, I L Simone, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
Human Genetics
|
February 6, 2010
Novel human pathological mutations. Gene symbol: SCN1A. Disease: Myoclonic epilepsy of infancy
F E Rocca, E V De Marco, F Annesi, et al.
Human Genetics
|
April 21, 2011
Novel human pathological mutations. Gene symbol: PARK7. Disease: Parkinson disease
P Tarantino, F Annesi, V Scornaienchi, et al.
BMC Bioinformatics
|
April 29, 2019
DNAscan: personal computer compatible NGS analysis, annotation and visualisation
A Iacoangeli, A Al Khleifat, W Sproviero, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 21, 2010
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis
F L Conforti, W Sproviero, I L Simone, et al.
Page
of 1