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Journal of Human Genetics|January 31, 2021
A loss-of-function variant in DNA mismatch repair gene MLH3 underlies severe oligozoospermiaShoaib Nawaz, Muhammad Imran Ullah, Beenish Samreen Hamid, et al.Genomics|March 10, 2020
Identification of a novel biallelic missense variant in the KIAA0825 underlies postaxial polydactyly type AAmir Hayat, Muhammad Umair, Safdar Abbas, et al.Human Genetics|November 8, 2005
Localization of a novel locus for alopecia with mental retardation syndrome to chromosome 3q26.33-q27.3Peter John, Ghazanfar Ali, Muhammad S Chishti, et al.Neurogenetics|April 23, 2022
A novel nonsense variant in EXOC8 underlies a neurodevelopmental disorderAsmat Ullah, Jai Krishin, Nighat Haider, et al.BMC Neurology|October 4, 2011
Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephalyRizwana Kousar, Muhammad Jawad Hassan, Bushra Khan, et al.Journal of Human Genetics|November 6, 2015
Homozygous sequence variants in the FKBP10 gene underlie osteogenesis imperfecta in consanguineous familiesMuhammad Umair, Annum Hassan, Abid Jan, et al.3 Biotech|July 29, 2022
Nephroprotective effect of polyphenol-rich extract of <i>Costus spicatus</i> in cisplatin-induced nephrotoxicity in Wistar albino ratsAmena Ali, Abuzer Ali, Wasim Ahmad, et al.Metabolic Brain Disease|March 9, 2019
Exploring the multifaceted neuroprotective actions of Emblica officinalis (Amla): a reviewIbraheem Husain, Saima Zameer, Tushar Madaan, et al.Journal of Human Genetics|December 18, 2007
Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani familiesMuhammad S Chishti, Attya Bhatti, Sana Tamim, et al.BMC Medical Genetics|February 28, 2014
A novel recessive mutation in the gene ELOVL4 causes a neuro-ichthyotic disorder with variable expressivityHina Mir, Syed Irfan Raza, Muhammad Touseef, et al.Pageof 34