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Showing results (141-150 of 144) with videos related to

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The Lancet. Neurology|December 3, 2013
The genetic basis of DOORS syndrome: an exome-sequencing studyPhilippe M Campeau, Dalia Kasperaviciute, James T Lu, et al.
Physical Review Letters|February 1, 2020
Fragmentation of Single-Particle Strength around the Doubly Magic Nucleus  ^{132}Sn and the Position of the 0f_{5/2} Proton-Hole State in ^{131}InV Vaquero, A Jungclaus, T Aumann, et al.
Brain : a Journal of Neurology|September 10, 2013
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1ADalia Kasperaviciute, Claudia B Catarino, Mar Matarin, et al.
Physical Review Letters|May 2, 2020
Extending the Southern Shore of the Island of Inversion to ^{28}FA Revel, O Sorlin, F M Marqués, et al.
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Showing results (141-150 of 144) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 144 results.
The Lancet. Neurology|December 3, 2013
The genetic basis of DOORS syndrome: an exome-sequencing studyPhilippe M Campeau, Dalia Kasperaviciute, James T Lu, et al.
Physical Review Letters|February 1, 2020
Fragmentation of Single-Particle Strength around the Doubly Magic Nucleus  ^{132}Sn and the Position of the 0f_{5/2} Proton-Hole State in ^{131}InV Vaquero, A Jungclaus, T Aumann, et al.
Brain : a Journal of Neurology|September 10, 2013
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1ADalia Kasperaviciute, Claudia B Catarino, Mar Matarin, et al.
Physical Review Letters|May 2, 2020
Extending the Southern Shore of the Island of Inversion to ^{28}FA Revel, O Sorlin, F M Marqués, et al.
Pageof 15