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M Raynaud

Showing results (61-70 of 64) with videos related to

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Molecular Psychiatry|December 21, 2011
Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disabilityL S Nguyen, L Jolly, C Shoubridge, et al.
Physical Review Letters|November 19, 2013
Evidence of resonant surface-wave excitation in the relativistic regime through measurements of proton acceleration from grating targetsT Ceccotti, V Floquet, A Sgattoni, et al.
Molecular Psychiatry|August 24, 2016
De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and femalesE E Palmer, T Stuhlmann, S Weinert, et al.
Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.
Pageof 7

Showing results (61-70 of 64) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 64 results.
Molecular Psychiatry|December 21, 2011
Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disabilityL S Nguyen, L Jolly, C Shoubridge, et al.
Physical Review Letters|November 19, 2013
Evidence of resonant surface-wave excitation in the relativistic regime through measurements of proton acceleration from grating targetsT Ceccotti, V Floquet, A Sgattoni, et al.
Molecular Psychiatry|August 24, 2016
De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and femalesE E Palmer, T Stuhlmann, S Weinert, et al.
Molecular Psychiatry|February 4, 2015
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesH Hu, S A Haas, J Chelly, et al.
Pageof 7