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Autor:
Mirghomizadeh F., Bardtke B., Devoto M., Pfister M., Oeken J., König S., Vitale E. 1, Riccio A., De Rienzo A., Zenner H.P., Blin N.
Publikováno v:
European journal of human genetics 10 (2002): 95–99.
info:cnr-pdr/source/autori:Mirghomizadeh F., Bardtke B., Devoto M., Pfister M., Oeken J., König S., Vitale E. 1, Riccio A., De Rienzo A., Zenner H.P., Blin N./titolo:Second family with hearing impairment linked to 19q13 and refined DFNA4 localization./doi:/rivista:European journal of human genetics/anno:2002/pagina_da:95/pagina_a:99/intervallo_pagine:95–99/volume:10
info:cnr-pdr/source/autori:Mirghomizadeh F., Bardtke B., Devoto M., Pfister M., Oeken J., König S., Vitale E. 1, Riccio A., De Rienzo A., Zenner H.P., Blin N./titolo:Second family with hearing impairment linked to 19q13 and refined DFNA4 localization./doi:/rivista:European journal of human genetics/anno:2002/pagina_da:95/pagina_a:99/intervallo_pagine:95–99/volume:10
Until now, over 30 loci have been identified by linkage analysis of affected families that segregate non-syndromic and dominantly inherited forms of hearing impairment (DFNA). A German family with a non-syndromic progressive hearing impairment transm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::9b591ac023003d7edad7270d3c094650
https://publications.cnr.it/doc/169663
https://publications.cnr.it/doc/169663