Zobrazeno 1 - 10
of 253
pro vyhledávání: '"Zenner, H.P."'
Autor:
Mirghomizadeh, F., Pfister, M. 1, Apaydin, F., Petit, C., Kupka, S., Pusch, C.M., Zenner, H.P., Blin, N.
Publikováno v:
In Neurobiology of Disease July 2002 10(2):157-164
Publikováno v:
Molecular and Cellular Biochemistry, 205, 25-37
Molecular and Cellular Biochemistry, 205, pp. 25-37
Molecular and Cellular Biochemistry, 205, pp. 25-37
Item does not contain fulltext
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
Autor:
Leal S.M., Apaydin F., Barnwell C., Iber M., Kandogan T., Cura O., Braendle O., Zenner H.P., Schwalb M., Vitale E.
Publikováno v:
European journal of human genetics (1998).
info:cnr-pdr/source/autori:Leal S.M., Apaydin F., Barnwell C., Iber M., Kandogan T.,Cura O., Braendle O., Zenner H.P., Schwalb M., Vitale E./titolo:Linkage studies of non syndromic recessive deafness in a Turkishkindred which segregates DFNB9./doi:/rivista:European journal of human genetics/anno:1998/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Leal S.M., Apaydin F., Barnwell C., Iber M., Kandogan T.,Cura O., Braendle O., Zenner H.P., Schwalb M., Vitale E./titolo:Linkage studies of non syndromic recessive deafness in a Turkishkindred which segregates DFNB9./doi:/rivista:European journal of human genetics/anno:1998/pagina_da:/pagina_a:/intervallo_pagine:/volume
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::b07dae5f800ae14a56fec5856c7507e3
https://publications.cnr.it/doc/19368
https://publications.cnr.it/doc/19368
Publikováno v:
HNO; Jul2014, Vol. 62 Issue 7, p520-524, 5p
Autor:
Zenner, H.P.
Publikováno v:
HNO; Mar2013, Vol. 61 Issue 3, p226-232, 7p
Totally Implantable Active Middle Ear Implants: Ten Years' Experience at the University of Tübingen.
Autor:
Zenner, H.P., Rodriguez Jorge, J.
Publikováno v:
Advances in Oto-Rhino-Laryngology; 2010, Vol. 69, p72-84, 13p
Autor:
Zenner, H.P.1 zenner@uni-tuebingen.de, Freitag, H.-G.2, Linti, C.3, Steinhardt, U., Rodriguez Jorge, J.1, Preyer, S.1, Mauz, P.-S.1, Sürth, M.3, Planck, H.3, Baumann, I.1, Lehner, R.4, Eiber, A.2
Publikováno v:
Hearing Research. Jun2004, Vol. 192 Issue 1/2, p36-46. 11p.
Publikováno v:
HNO; Dec2002, Vol. 50 Issue 12, p1068-1074, 7p
Autor:
Helms, J., Müller, J., Schön, F., Winkler, F., Moser, L., Shehata-Dieler, W., Kastenbauer, E., Baumann, U., Rasp, G., Schorn, K., Eβer, B., Baumgartner, W., Hamzavi, S., Gstöttner, W., Westhofen, M., Döring, W., Dujardin, H., Albegger, K., Mair, A., Zenner, H.P.
Publikováno v:
ORL; 2001, Vol. 63 Issue 1, p31-40, 10p