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British Journal of Cancer|December 9, 2022
Efficacy and toxicity of primary re-irradiation for malignant spinal cord compression based on radiobiological modelling: a phase II clinical trialNeil D Wallace, Mary T Dunne, Orla McArdle, et al.American Journal of Medical Genetics. Part A|August 5, 2017
Identification of STAC3 variants in non-Native American families with overlapping features of Carey-Fineman-Ziter syndrome and Moebius syndromeAida Telegrafi, Bryn D Webb, Sarah M Robbins, et al.American Journal of Medical Genetics. Part A|July 24, 2012
Nablus mask-like facial syndrome: deletion of chromosome 8q22.1 is necessary but not sufficient to cause the phenotypeJudith Allanson, Amanda Smith, Heather Hare, et al.Human Genetics|August 10, 2006
Clinical and molecular genetic features of ARC syndromePaul Gissen, Louise Tee, Colin A Johnson, et al.Journal of Medical Genetics|August 10, 2014
The clinical significance of small copy number variants in neurodevelopmental disordersReza Asadollahi, Beatrice Oneda, Pascal Joset, et al.Nature Methods|March 2, 2019
Author Correction: Stability, affinity, and chromatic variants of the glutamate sensor iGluSnFRJonathan S Marvin, Benjamin Scholl, Daniel E Wilson, et al.Nature Methods|November 1, 2018
Stability, affinity, and chromatic variants of the glutamate sensor iGluSnFRJonathan S Marvin, Benjamin Scholl, Daniel E Wilson, et al.Epilepsia|February 7, 2017
Heterozygous truncation mutations of the SMC1A gene cause a severe early onset epilepsy with cluster seizures in females: Detailed phenotyping of 10 new casesJoseph D Symonds, Shelagh Joss, Kay A Metcalfe, et al.Nature Methods|January 4, 2019
Publisher Correction: Stability, affinity, and chromatic variants of the glutamate sensor iGluSnFRJonathan S Marvin, Benjamin Scholl, Daniel E Wilson, et al.Brain : a Journal of Neurology|February 9, 2022
Activating RAC1 variants in the switch II region cause a developmental syndrome and alter neuronal morphologySiddharth Banka, Abigail Bennington, Martin J Baker, et al.Pageof 15