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, 2023
Carlo 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, 2020
Fatemeh Azadegan   +2 more
exaly  

Absence of deafness-associated connexin-26 (GJB2) gene mutations in the Omani population

Human Mutation, 2001
Muralitharan Shanmugakonar, M Simsek
exaly  

GJB2 gene mutations in Syrians with sensorineural hearing loss

Middle East Journal of Medical Genetics, 2012
Zeina N. Mahayri, Fawza S. Monem
openaire   +1 more source

Selective Heterozygous Advantage of Carriers of с.-23+1G>A Mutation in GJB2 Gene Causing Autosomal Recessive Deafness 1A

Bulletin of Experimental Biology and Medicine, 2019
Georgiĭ Romanov   +2 more
exaly  

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