Zobrazeno 1 - 10
of 624
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
Autor:
Liu, Bin1,2 (AUTHOR) liubin159@shu.edu.cn, Liang, Junyi3 (AUTHOR) liangj3@ccf.org, Yao, Wenjuan1,2 (AUTHOR) liangj3@ccf.org, Xu, Chun4 (AUTHOR) imxuchun@sjtu.edu.cn
Publikováno v:
Mathematics (2227-7390). Aug2024, Vol. 12 Issue 16, p2470. 17p.
Autor:
Kosugi, Yuki1 (AUTHOR) yukikosugi@outlook.jp, Miwa, Toru1,2 (AUTHOR) miw.com1101@gmail.com, Haruta, Yuka1 (AUTHOR) hashimoto@ent-ocu.com, Hashimoto, Kosuke1 (AUTHOR) shoko.kato@omu.ac.jp, Kato, Shoko1 (AUTHOR)
Publikováno v:
Audiology Research. Aug2024, Vol. 14 Issue 4, p674-683. 10p.
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:
Binazzi, Alessandra1 (AUTHOR) a.binazzi@inail.it, di Marzio, Davide1 (AUTHOR) a.marinaccio@inail.it, Mensi, Carolina2 (AUTHOR) carolina.mensi@unimi.it, Consonni, Dario2 (AUTHOR) dario.consonni@unimi.it, Miligi, Lucia3,4 (AUTHOR) l.miligi@ispro.toscana.it, Piro, Sara4 (AUTHOR), Zajacovà, Jana5 (AUTHOR) jana.zajacova@aslcn1.it, Sorasio, Denise5 (AUTHOR) denise.sorasio@aslcn1.it, Galli, Paolo6 (AUTHOR) paolo.galli@ausl.bologna.it, Camagni, Angela6 (AUTHOR) angela.camagni@ausl.bologna.it, Calisti, Roberto7 (AUTHOR) roberto.calisti@sanita.marche.it, Massacesi, Stefania7 (AUTHOR) stefania.massacesi@sanita.marche.it, Cozzi, Ilaria8,9 (AUTHOR) i.cozzi@deplazio.it, Balestri, Anna8,9 (AUTHOR) anna.balestri@asl.vt.it, Murano, Stefano10 (AUTHOR) stefano.murano@sabes.it, Fedeli, Ugo11 (AUTHOR) ugo.fedeli@azero.veneto.it, Comiati, Vera11 (AUTHOR) vera.comiati@azero.veneto.it, Eccher, Silvia12 (AUTHOR) silvia.eccher@apss.tn.it, Lattanzio, Sara12 (AUTHOR) sara.lattanzio@apss.tn.it, Marinaccio, Alessandro1 (AUTHOR)
Publikováno v:
Cancers. Jun2024, Vol. 16 Issue 11, p2053. 12p.
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:
ORL; 1986, Vol. 48 Issue 2, p68-75, 8p
Publikováno v:
HNO; Jul2014, Vol. 62 Issue 7, p520-524, 5p
Autor:
Jain, Kinshuk1 (AUTHOR) kinshuk.jain21@imperial.ac.uk, McCarley, Sarah C.1 (AUTHOR) sarah.mccarley22@imperial.ac.uk, Mukhtar, Ghazel1 (AUTHOR) ghazel.mukhtar18@imperial.ac.uk, Ferlin, Anna2 (AUTHOR) a.ferlin@rbht.nhs.uk, Fleming, Andrew2 (AUTHOR) a.fleming@rbht.nhs.uk, Morris-Rosendahl, Deborah J.1,2 (AUTHOR) d.morris-rosendahl@rbht.nhs.uk, Shovlin, Claire L.1,3,4 (AUTHOR) c.shovlin@imperial.ac.uk
Publikováno v:
Journal of Clinical Medicine. Jan2024, Vol. 13 Issue 1, p250. 19p.