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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Counseling and POU3F4[original query]
Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations.
BMC medical genetics 2015 16 9.
Bademci Guney, Lasisi Akeem, Yariz Kemal O, Montenegro Paola, Menendez Ibis, Vinueza Rodrigo, Paredes Rosario, Moreta Germania, Subasioglu Asli, Blanton Susan, Fitoz Suat, Incesulu Armagan, Sennaroglu Levent, Tekin Musta
Hereditary etiology of non-syndromic sensorineural hearing loss in the Republic of North Ossetia-Alania.
PeerJ 2023 2 11 e14514.
Petrova Nika, Tebieva Inna, Kadyshev Vitaly, Getoeva Zalina, Balinova Natalia, Marakhonov Andrey, Vasilyeva Tatyana, Ginter Evgeny, Kutsev Sergey, Zinchenko Re
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