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Scientific Reports|October 14, 2022
Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucomaBushra Rauf, Shahid Y Khan, Xiaodong Jiao, et al.European Journal of Human Genetics : EJHG|July 16, 2009
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3Shahid Yar Khan, Saima Riazuddin, Mohsin Shahzad, et al.Molecular Vision|May 2, 2020
Mutations in FYCO1 identified in families with congenital cataractsHira Iqbal, Shahid Y Khan, Lin Zhou, et al.Research in Microbiology|September 10, 2022
Genomic analysis of Chryseobacterium indologenes and conformational dynamics of the selected DD-peptidaseMuhammad Irfan, Muhammad Tariq, Zarrin Basharat, et al.Journal of Human Genetics|June 3, 2011
Molecular and clinical studies of X-linked deafness among Pakistani familiesAli M Waryah, Zubair M Ahmed, Munir A Bhinder, et al.American Journal of Human Genetics|February 23, 2010
Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79Atteeq Ur Rehman, Robert J Morell, Inna A Belyantseva, et al.Genes|April 3, 2021
Genetic Causes of Oculocutaneous Albinism in Pakistani PopulationZureesha Sajid, Sairah Yousaf, Yar M Waryah, et al.Human Genetics|June 21, 2020
Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing lossKevin T Booth, Amama Ghaffar, Muhammad Rashid, et al.Scientific Reports|March 8, 2017
Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani populationMohsin Shahzad, Sairah Yousaf, Yar M Waryah, et al.Archives of Medical Research|March 6, 2012
Targeted next generation sequencing reveals a novel intragenic deletion of the TPO gene in a family with intellectual disabilityZafar Iqbal, Kornelia Neveling, Attia Razzaq, et al.Pageof 5