New gene for automosol recessive non-syndromic hearing loss maps to either chromosome 3q or 19p

Autor:	Chen, A., Wayne, S., Bell, A., Ramesh, A., Srisailapathy, C. R. S., Scott, D. A., Val Sheffield, Hauwe, P., Zbar, R. I. S., Ashley, J., Lovett, M., Camp, G., Smith, R. J. H.
Zdroj:	Scopus-Elsevier
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::885fdb42128d0067823baf1942d0e8d7 http://www.scopus.com/inward/record.url?eid=2-s2.0-0030796428&partnerID=MN8TOARS Zobrazit plný text záznamu