Suchergebnisse - "GJB3 protein, human"

PubPharm (171)

1

Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China

enthalten in: International journal of pediatric otorhinolaryngology | 2024

von Xiong, Y. | Chen, M. | Wang, H. | +3

2

Concurrent Hearing and Genetic Screening among Newborns in Ningbo, China

enthalten in: Computational and mathematical methods in medicine | 2022

von Guomei, C. | Luyan, Z. | Lingling, D. | +2

RetractionIn: Comput Math Methods Med. 2023 Dec 6;2023:9758034. - PMID 38094399

3

Genetic Susceptibility Study of Chinese Sudden Sensorineural Hearing Loss Patients with Vertigo

enthalten in: Current medical science | 2021

von Gao, Y. | Wang, H. | Guan, J. | +5

4

Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China

enthalten in: Medicine | 2021

von Hu, H. | Zhou, P. | Wu, J. | +4

5

Genetic etiology study of four Chinese families with two nonsyndromic deaf children in succession by targeted next-generation sequencing

enthalten in: Molecular genetics & genomic medicine | 2021

von Xiao, C. | Liu, S. | Wang, H. | +3

6

Expanding the clinical phenotype associated with NIPAL4 mutation : Study of a Tunisian consanguineous family with erythrokeratodermia variabilis-Like Autosomal Recessive Congenital Ichthyosis

enthalten in: PloS one | 2021

von Charfeddine, C. | Laroussi, N. | Mkaouar, R. | +10

7

Comparative Analysis of Cx31 and Cx43 in Differentiation-Competent Rodent Keratinocytes

enthalten in: Biomolecules | 2020

von Au, A. | Shao, Q. | White, K. | +4

8

The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest China

enthalten in: International journal of pediatric otorhinolaryngology | 2020

von Liu, X. | Wang, J. | Wang, S. | +7

9

Analysis of prenatal phenotype and pathogenetic variant in a fetus with Papillorenal syndrome

enthalten in: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020

von Zhao, X. | Yang, D. | Jia, Y. | +13

10

Analysis of deafness gene variant screening of 7875 neonatal cases in Dongying area of Shandong

enthalten in: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2020

von Tian, M. | Cao, Y. | Chen, Z. | +5

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