Results 151 to 160 of about 5,521 (170)
Some of the next articles are maybe not open access.
Posterior Cranial Fossa Malformation and Vascular Dysplasia in GJB2 Gene Mutation
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 2023Carlo Alberto Cesaroni +5 more
openaire +2 more sources
GJB2‐related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations
Annals of Human Genetics, 2020Fatemeh Azadegan +2 more
exaly
The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)
Genes, 2023Vera Pshennikova +2 more
exaly
Absence of deafness-associated connexin-26 (GJB2) gene mutations in the Omani population
Human Mutation, 2001Muralitharan Shanmugakonar, M Simsek
exaly
GJB2 gene mutations in Syrians with sensorineural hearing loss
Middle East Journal of Medical Genetics, 2012Zeina N. Mahayri, Fawza S. Monem
openaire +1 more source

