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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Counseling and CDH23[original query]
The homozygous p.V37I variant of GJB2 is associated with diverse hearing phenotypes.
Clinical genetics 2015 Apr 87 (4): 350-5.
Chai Y, Chen D, Sun L, Li L, Chen Y, Pang X, Zhang L, Wu H, Yang
Whole exome sequencing of six Chinese families with hereditary non-syndromic hearing loss.
International journal of pediatric otorhinolaryngology 2021 7 148 110817.
Liang Pengfei, Chen Fengping, Wang Shujuan, Li Qiong, Li Wei, Wang Jian, Chen Jun, Zha Dingj
Whole-Exome Sequencing Reveals a Rare Variant of OTOF Gene Causing Congenital Non-syndromic Hearing Loss Among Large Muslim Families Favoring Consanguinity.
Frontiers in genetics 2021 6 12 641925.
Fareed Mohd, Sharma Varun, Singh Inderpal, Rehman Sayeed Ur, Singh Gurdarshan, Afzal Mohamm
Cochlear Implantation Outcomes in Children With CDH23 Mutations-Associated Hearing Loss.
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2021 11 167 (3): 560-565.
Chen Kaitian, Huang Bixue, Sun Jincangjian, Liang Yue, Xiong Guanx
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
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