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Plos One|June 20, 2024
Exploring the effects of noise pollution on physiology and ptilochronology of birdsRida Amjad, Tahira Ruby, Kashif Ali, et al.Saudi Journal of Biological Sciences|February 24, 2022
Therapeutic Potential of Selected Medicinal Plant Extracts against Multi-Drug Resistant Salmonella enterica serovar TyphiSadaf Naz, Sadia Alam, Waseem Ahmed, et al.Human Molecular Genetics|January 3, 2018
CDC14A phosphatase is essential for hearing and male fertility in mouse and humanAyesha Imtiaz, Inna A Belyantseva, Alisha J Beirl, et al.JAMA Neurology|May 24, 2013
A novel OPA3 mutation revealed by exome sequencing: an example of reverse phenotypingBeenish Arif, Kishore R Kumar, Philip Seibler, et al.Journal of Medical Genetics|May 23, 2020
Bi-allelic TTC5 variants cause delayed developmental milestones and intellectual disabilityArisha Rasheed, Evren Gumus, Maha Zaki, et al.Human Mutation|November 30, 2020
Biallelic TMEM251 variants in patients with severe skeletal dysplasia and extreme short statureNoor U Ain, Niaz Muhammad, Mehdi Dianatpour, et al.American Journal of Human Genetics|July 30, 2002
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locusSadaf Naz, Chantal M Giguere, David C Kohrman, et al.Journal of Neurology|November 9, 2013
Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutationSarah Doss, Katja Lohmann, Philip Seibler, et al.Medrxiv : the Preprint Server for Health Sciences|October 24, 2023
PKHD1L1, A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing LossShelby E Redfield, Pedro De-la-Torre, Mina Zamani, et al.Human Genetics|March 8, 2024
PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing lossShelby E Redfield, Pedro De-la-Torre, Mina Zamani, et al.Pageof 12