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Journal of Human Genetics|November 1, 2013
Novel mutation in AAA domain of BCS1L causing Bjornstad syndromeSaima Siddiqi, Saadat Siddiq, Atika Mansoor, et al.Frontiers in Genetics|March 21, 2019
A Novel Homozygous Frameshift Variant in XYLT2 Causes Spondyloocular Syndrome in a Consanguineous Pakistani FamilyMehran Kausar, Elaine Guo Yan Chew, Hazrat Ullah, et al.BMC Medical Genetics|December 15, 2017
Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani familyMuhammad Ajmal, Asif Mir, Sughra Wahid, et al.Human Genetics|February 27, 2004
Investigation of the Greek ancestry of populations from northern PakistanAtika Mansoor, Kehkashan Mazhar, Shagufta Khaliq, et al.BMC Medicine|March 7, 2017
Genetics of vascular dementia - review from the ICVD working groupM Arfan Ikram, Anna Bersano, Raquel Manso-Calderón, et al.Frontiers in Neurology|November 7, 2022
Case report: Expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental diseaseEthiraj Ravindran, Noor Ullah, Shyamala Mani, et al.Biochimica Et Biophysica Acta|January 20, 2004
Genetic instability in EBV-transformed lymphoblastoid cell linesAisha Mohyuddin, Qasim Ayub, Saima Siddiqi, et al.Virology Journal|December 11, 2013
Study of PKRBD in HCV genotype 3a infected patients in response to interferon therapy in Pakistani populationAtika Mansoor, Lubna Ali, Noor-ul Sabah, et al.Transboundary and Emerging Diseases|May 5, 2022
Genome sequencing and analysis of genomic diversity in the locally transmitted SARS-CoV-2 in PakistanMuhammad Shakeel, Muhammad Irfan, Zaib Un Nisa, et al.American Journal of Physical Anthropology|October 9, 2003
Reconstruction of human evolutionary tree using polymorphic autosomal microsatellitesQasim Ayub, Atika Mansoor, Muhammad Ismail, et al.Pageof 4