Ultrasensitive deafness gene DNA hybridization detection employing a fiber optic Mach-Zehnder interferometer: Enabled by a black phosphorus nanointerface
L Wang, D Yi, Y Geng, T Duan, Z Tong, S Chen… - Biosensors and …, 2023 - Elsevier
The rapid and efficient detection of deafness gene DNA plays an important role in the
clinical diagnosis of deafness diseases. This study demonstrates the ultrasensitive detection …
clinical diagnosis of deafness diseases. This study demonstrates the ultrasensitive detection …
[PDF][PDF] Do we really need genetic tests in current clinical practice?
C Bănescu - Revista Romana de Medicina de Laborator, 2019 - sciendo.com
Currently there is an increased number of genetic tests available for disorders produced by
chromosomal or gene abnormalities. Some genetic tests are recommended by healthcare …
chromosomal or gene abnormalities. Some genetic tests are recommended by healthcare …
Identification of novel microsatellite markers flanking GJB2 gene in order to use in preimplantation genetic diagnosis of hearing loss: A comparison of whole-genome …
Z Tabatabaei, MAF Fard, SB Hashemi… - European journal of …, 2020 - Elsevier
Hearing loss is the most prevalent sensorineural disorder which can be caused by genetic
factors in more than half of the cases. GJB2 mutations with the frequency of 18.7% are the …
factors in more than half of the cases. GJB2 mutations with the frequency of 18.7% are the …
[HTML][HTML] Connexin 26 (GJB2) gene mutations linked with autosomal recessive non-syndromic sensor neural hearing loss in the Iraqi population
AM Al-Janabi, HS Ahmmed… - Journal of Medicine and …, 2021 - ncbi.nlm.nih.gov
Deafness is a total or partial hearing loss that may appear at any age and with different
degrees of severity. Approximately 50% of hearing loss have a genetic origin, and among …
degrees of severity. Approximately 50% of hearing loss have a genetic origin, and among …
Genetic testing in pediatrics-a narrative essay of challenges and possibilities in Romania
C Duicu - Revista Romana de Medicina de Laborator, 2019 - sciendo.com
In spite of extensive medical examinations, many pediatric patients remain without a clear
diagnosis. The genetic testing is necessary in the evaluation of some of these challenging …
diagnosis. The genetic testing is necessary in the evaluation of some of these challenging …
Audiological features in Serbian patients with hearing impairment identified with c. 35delG in the GJB2 gene
B Dobrić, D Radivojević, J Ječmenica… - Srpski arhiv za …, 2021 - doiserbia.nb.rs
Introduction/Objective. Hearing impairment is the most common sensorineural disorder with
an incidence of 1/700–1000 newborns. Variants in the GJB2 gene are the major cause of …
an incidence of 1/700–1000 newborns. Variants in the GJB2 gene are the major cause of …
[PDF][PDF] Relevance of Connexin 26 (GJB2) Gene Mutations With Congenital Nonsyndromic Sensorineural Hearing Loss in Lraqi Deafness Patients.
AM Al-janabi, HS Ahmmed, SM Alkhafaji - 2021 - scholar.archive.org
Objective: This study aimed to detect the frequency of the three most common mutations of
GJB2 in nonsyndromic sensorineural deafness for Iraqi population. Method: The current …
GJB2 in nonsyndromic sensorineural deafness for Iraqi population. Method: The current …
[引用][C] Audiološke karakteristike kod bolesnika iz Srbije sa oštećenjem sluha sa identifikovanom mutacijom c. 35delG gena GJB2
B Dobrić, D Radivojević… - Srpski arhiv za …, 2021 - Serbian Medical Society, Belgrade