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Journal of Psychiatry & Neuroscience : JPN|November 1, 2022
RGS3 and IL1RAPL1 missense variants implicate defective neurotransmission in early-onset inherited schizophreniasAmbreen Kanwal, José V Pardo, Sadaf NazBiology|April 13, 2026
Genetic Variants from Large Cohorts and Familial Studies Implicate Common Mechanisms in SchizophreniaAmbreen Kanwal, José V Pardo, Sadaf NazJournal of Medical Genetics|August 24, 2017
Autosomal recessive chondrodysplasia with severe short stature caused by a biallelic COL10A1 variantNoor Ul Ain, Outi Makitie, Sadaf NazPakistan Journal of Medical Sciences|March 16, 2026
Randomized controlled trial to compare functional outcomes between Locking compression Plates and Retrograde Intramedullary Nails in distal femur fracturesAimal Sattar, Ayesha Imtiaz, Syed Imran BukhariEuropean Journal of Medical Genetics|September 16, 2019
RIN2 and BBS7 variants as cause of a coincidental syndromeMemoona Shaukat, Tayyaba Ishaq, Niaz Muhammad, et al.Gene|May 24, 2012
A p.C343S missense mutation in PJVK causes progressive hearing lossGhulam Mujtaba, Ihtisham Bukhari, Amara Fatima, et al.International Journal of Biological Macromolecules|December 3, 2023
Applications of guar gum polysaccharide for pharmaceutical drug delivery: A reviewNyla Amjed, Muhammad Zeshan, Ariba Farooq, et al.BMC Musculoskeletal Disorders|July 21, 2021
RAB33B and PCNT variants in two Pakistani families with skeletal dysplasia and short statureNoor Ul Ain, Zunaira Fatima, Sadaf Naz, et al.International Journal of Intelligent Systems|July 31, 2023
A comprehensive review of federated learning for COVID-19 detectionSadaf Naz, Khoa T Phan, Yi-Ping Phoebe ChenGene|July 13, 2015
Homozygous p.G61E mutation in a consanguineous Pakistani family with co-existence of juvenile-onset open angle glaucoma and primary congenital glaucomaRasheeda Bashir, Hafsa Tahir, Khazeema Yousaf, et al.Pageof 12