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Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|November 14, 2024
Increase in blood derived mitochondrial DNA copy number in strabismus patientsZainab Zehra, Muhammad Amn Zia, Sorath Noorani Siddiqui, et al.
Journal of Human Genetics|October 10, 2014
A canonical splice site mutation in GIPC3 causes sensorineural hearing loss in a large Pakistani familySaima Siddiqi, Muhammad Ismail, Jaap Oostrik, et al.
Molecular Biology Reports|March 11, 2010
Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemiaMuhammad Ajmal, Waqas Ahmed, Ahmed Sadeque, et al.
Molecular Vision|December 24, 2009
Association of tumor necrosis factor alpha gene polymorphism G-308A with pseudoexfoliative glaucoma in the Pakistani populationMuhammad Imran Khan, Shazia Micheal, Noreen Rana, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 29, 2013
The genetic spectrum of familial hypercholesterolemia in PakistanWaqas Ahmed, Ros Whittall, Moeen Riaz, et al.
Molecular Vision|November 7, 2022
Association of IGF1 polymorphisms with exotropia in a Pakistani cohortZainab Zehra, Netasha Khan, Minhal Nadeem, et al.
The International Journal of Neuroscience|August 29, 2023
Association of 11 variants of the dopaminergic and cognitive pathways genes with major depression, schizophrenia and bipolar disorder in the Pakistani populationAisha Nasir Hashmi, Merlyn Sabina Raja, Rizwan Taj, et al.
European Archives of Psychiatry and Clinical Neuroscience|December 30, 2022
Contributing risk factors of common psychiatric disorders in the Pakistani populationAisha Nasir Hashmi, Raheel Qamar, Rizwan Taj, et al.
Molecular Vision|May 19, 2012
Role of Lysyl oxidase-like 1 gene polymorphisms in Pakistani patients with pseudoexfoliative glaucomaShazia Micheal, Muhammad Imran Khan, Farah Akhtar, et al.
Genetics Research|October 7, 2015
A de novo microdeletion in NRXN1 in a Dutch patient with mild intellectual disability, microcephaly and gonadal dysgenesisZehra Agha, Zafar Iqbal, Tjitske Kleefstra, et al.
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