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Molecular Psychiatry
|
May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders
O Mercati, G Huguet, A Danckaert, et al.
Brain : a Journal of Neurology
|
February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutations
P Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Neurogenetics
|
March 8, 2018
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype
T Smol, F Petit, A Piton, et al.
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of 15
Search research articles
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Showing results (141-150 of 143) with videos related to
Sort By:
Page
of 15
You have reached the last page of results.
This site can display upto 143 results.
Molecular Psychiatry
|
May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders
O Mercati, G Huguet, A Danckaert, et al.
Brain : a Journal of Neurology
|
February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutations
P Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Neurogenetics
|
March 8, 2018
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype
T Smol, F Petit, A Piton, et al.
Page
of 15