Showing results (11-20 of 20) with videos related to
Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Pakistan Journal of Pharmaceutical Sciences|November 16, 2020
Effect of paroxetine on intestinal motility in the presence of ondansetronAyesha Afzal, Ammara Khan, Asma Khan, et al.Pathology|October 13, 2017
The value of endomyocardial biopsy in diagnosis and guiding therapyTayyaba Khan, Dinesh Selvakumar, Siddharth Trivedi, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|September 12, 2021
FISH analysis of brain smears obtained at intraoperative diagnosis - An accurate and fast method to detect 1p/19q-codeletion in gliomasJoanne Brown, Sally Byatt, Tayyaba Khan, et al.Pediatric Research|September 27, 2022
Pharmacogenetic profiling via genome sequencing in children with medical complexityAmy Pan, Sierra Scodellaro, Tayyaba Khan, et al.American Journal of Medical Genetics. Part A|June 23, 2021
Genome sequencing for detection of pathogenic deep intronic variation: A clinical case report illustrating opportunities and challengesSusan Walker, Sylvia Lamoureux, Tayyaba Khan, et al.American Journal of Human Genetics|March 29, 2023
Trio RNA sequencing in a cohort of medically complex childrenAshish R Deshwar, Kyoko E Yuki, Huayun Hou, et al.Case Reports in Infectious Diseases|April 3, 2023
A Case Report of Acute Severe Necrotizing Pancreatitis following the Johnson & Johnson Vaccine against the Novel SARS-CoV-2Ayrton I Bangolo, Mahabuba Akhter, Auda Auda, et al.The Lancet. Neurology|August 18, 2023
Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort studyAlissa M D'Gama, Sarah Mulhern, Beth R Sheidley, et al.Brain : a Journal of Neurology|July 19, 2022
Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypesMarcello Scala, Masashi Nishikawa, Hidenori Ito, et al.The Journal of Clinical Investigation|November 14, 2023
Spliceosome malfunction causes neurodevelopmental disorders with overlapping featuresDong Li, Qin Wang, Allan Bayat, et al.Pageof 2