Records 1 - 3
| Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria.
European journal of human genetics : EJHG 2021 Nov .
Adeyemo Adebolajo, Faridi Rabia, Chattaraj Parna, Yousaf Rizwan, Tona Risa, Okorie Samuel, Bharadwaj Thashi, Nouel-Saied Liz M, Acharya Anushree, Schrauwen Isabelle, Morell Robert J, Leal Suzanne M, Friedman Thomas B, Griffith Andrew J, Roux Isabel
| Whole exome sequencing identifies a pathogenic mutation in WFS1 in two large Chinese families with autosomal dominant all-frequency hearing loss and prenatal counseling.
International journal of pediatric otorhinolaryngology 2018 Mar 106 113-119.
Cheng Hongbo, Zhang Qin, Wang Wenbin, Meng Qingxia, Wang Fuxin, Liu Minjuan, Mao Jun, Shi Yichao, Wang Wei, Li Ho
| Genotypic classification of patients with Wolfram syndrome: insights into the natural history of the disease and correlation with phenotype.
Genetics in medicine : official journal of the American College of Medical Genetics 2013 Jul 15 (7): 497-506.
de Heredia Miguel López, Clèries Ramón, Nunes Virgin