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Cochlear Implants International|April 17, 2009
The transmeatal approach: a new technique in cochlear and middle ear implantsKhalid TaibahGene|March 21, 2013
Homozygosity mapping identifies a novel GIPC3 mutation causing congenital nonsyndromic hearing loss in a Saudi familyKhushnooda Ramzan, Mohammed Al-Owain, Rabab Allam, et al.International Journal of Pediatric Otorhinolaryngology|January 9, 2014
COL4A4-related nephropathy caused by a novel mutation in a large consanguineous Saudi familyKhushnooda Ramzan, Faiqa Imtiaz, Khalid Taibah, et al.The Journal of Laryngology and Otology|October 23, 2002
Obstructive endotracheal lesions of thyroid cancerMohammed Ahmed, Muhammad Saleem, Abdullah Al-Arifi, et al.European Journal of Medical Genetics|April 29, 2014
ILDR1: Novel mutation and a rare cause of congenital deafness in the Saudi Arabian populationKhushnooda Ramzan, Khalid Taibah, Asma I Tahir, et al.Molecular Vision|August 10, 2012
USH1G with unique retinal findings caused by a novel truncating mutation identified by genome-wide linkage analysisFaiqa Imtiaz, Khalid Taibah, Ghada Bin-Khamis, et al.BMC Medical Genetics|July 6, 2011
A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian populationFaiqa Imtiaz, Khalid Taibah, Khushnooda Ramzan, et al.Nature Medicine|March 17, 2023
Genetic association analysis of 77,539 genomes reveals rare disease etiologiesDaniel Greene, , Daniela Pirri, et al.Pageof 1