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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 13, 2024. (Total: 234352Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Syndrome and GJB3[original query]
[The roles of connexin genes in sporadic hearing loss population].
Zhonghua yi xue za zhi 2007 Apr 87 (16): 1097-101.
Li Qing-zhong, Wang Qiu-ju, Chi Fang-lu, Li Li-na, Zhao Ya-li, Yuan Hu, Han Dong-
Genetic analysis of presbycusis by arrayed primer extension.
Annals of clinical and laboratory science 2008 38 (4): 352-60.
Rodriguez-Paris Juan, Ballay Charles, Inserra Michelle, Stidham Katrina, Colen Tahl, Roberson Joseph, Gardner Phyllis, Schrijver Ir
Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss.
International journal of pediatric otorhinolaryngology 2009 Jan 73 (1): 103-7.
Teek Rita, Oitmaa Eneli, Kruustük Katrin, Zordania Riina, Joost Kairit, Raukas Elve, Tõnisson Neeme, Gardner Phyllis, Schrijver Iris, Kull Mart, Ounap Katr
Evidence for the absence of mutations at GJB3, GJB4 and LOR in progressive symmetrical erythrokeratodermia.
Clinical and experimental dermatology 2011 Jun 36 (4): 399-405.
Wei S, Zhou Y, Zhang T D, Huang Z M, Zhang X B, Zhu H L, Liang B H, Lin L, Deng
Genotypes and phenotypes of a family with a deaf child carrying combined heterozygous mutations in SLC26A4 and GJB3 genes.
Molecular medicine reports 2016 May .
Li Yunlong, Zhu Baoshe
Hearing-loss-associated gene detection in neonatal intensive care unit.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2017 Jan 1-12.
Yang S M, Liu Ying, Liu C, Yin A H, Wu Y F, Zheng X E, Yang H M, Yang
[An analysis of the mutation in GJB2?GJB3?SLC26A4 and mtDNA12SrRNA in new born].
Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery 2017 May 31 (9): 664-666.
Chai F, Zhao H L, Qiu S
Whole-Exome Sequencing Targeting a Gene Panel for Sensorineural Hearing Loss: The First Portuguese Cohort Study.
Cytogenetic and genome research 2022 5 162 (1-2): 1-9.
Reis Cláudia Sousa, Quental Sofia, Fernandes Susana, Castedo Sérgio, Moura Carla Pin
[Genetic analysis of a Chinese pedigree featuring non-simplex blepharocheilodontic syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 12 40 (1): 36-41.
Yan Lulu, Liu Yingwen, Zhang Yuxin, Tian Liyun, Cao Juan, Li Hai
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