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N Mohammed

Showing results (251-260 of 255) with videos related to

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IEEE Transactions on Geoscience and Remote Sensing : a Publication of the IEEE Geoscience and Remote Sensing Society|July 15, 2020
SMAP L-Band Microwave Radiometer: Instrument Design and First Year on OrbitJeffrey R Piepmeier, Paolo Focardi, Kevin A Horgan, et al.
Frontiers in Neurology|September 7, 2021
Pathogenic Variants in <i>ABHD16A</i> Cause a Novel Psychomotor Developmental Disorder With Spastic ParaplegiaAshraf Yahia, Liena E O Elsayed, Remi Valter, et al.
European Journal of Human Genetics : EJHG|February 5, 2024
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile EpilepsyMahmoud Koko, Maha A Elseed, Inaam N Mohammed, et al.
European Journal of Human Genetics : EJHG|September 8, 2016
Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in SudanLiena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, et al.
European Journal of Human Genetics : EJHG|December 1, 2011
How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrumSiddharth Banka, Ratna Veeramachaneni, William Reardon, et al.
Pageof 26

Showing results (251-260 of 255) with videos related to

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Pageof 26
You have reached the last page of results.This site can display upto 255 results.
IEEE Transactions on Geoscience and Remote Sensing : a Publication of the IEEE Geoscience and Remote Sensing Society|July 15, 2020
SMAP L-Band Microwave Radiometer: Instrument Design and First Year on OrbitJeffrey R Piepmeier, Paolo Focardi, Kevin A Horgan, et al.
Frontiers in Neurology|September 7, 2021
Pathogenic Variants in <i>ABHD16A</i> Cause a Novel Psychomotor Developmental Disorder With Spastic ParaplegiaAshraf Yahia, Liena E O Elsayed, Remi Valter, et al.
European Journal of Human Genetics : EJHG|February 5, 2024
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile EpilepsyMahmoud Koko, Maha A Elseed, Inaam N Mohammed, et al.
European Journal of Human Genetics : EJHG|September 8, 2016
Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in SudanLiena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, et al.
European Journal of Human Genetics : EJHG|December 1, 2011
How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrumSiddharth Banka, Ratna Veeramachaneni, William Reardon, et al.
Pageof 26