Zobrazeno 1 - 3
of 3
pro vyhledávání: '"L V, Gallo"'
Autor:
Martina Beltramello, Giuseppe Chiarella, Miranda Menniti, Nicola Perrotti, Fabio Mammano, M. Catalano, R Argento, L. V. Gallo, Emma Colao, Valeria Piazza, Ettore Cassandro, Paola Malatesta
Publikováno v:
Clinical Genetics. 68:161-166
Mutations in the gene (GJB2) coding for Connexin 26 (Cx26) are responsible for genetic forms of sensorineural hearing loss. This article describes a family characterized by congenital profound hearing loss, inherited in an autosomal dominant fashion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb6d06ed1c2da1f11ba0f6d2140cd3ff
https://doi.org/10.1111/j.1399-0004.2005.00468.x
https://doi.org/10.1111/j.1399-0004.2005.00468.x
Autor:
V, Piazza, M, Beltramello, M, Menniti, E, Colao, P, Malatesta, R, Argento, G, Chiarella, L V, Gallo, M, Catalano, N, Perrotti, F, Mammano, E, Cassandro
Mutations in the gene (GJB2) coding for Connexin 26 (Cx26) are responsible for genetic forms of sensorineural hearing loss. This article describes a family characterized by congenital profound hearing loss, inherited in an autosomal dominant fashion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1d54c5c1edc2e3921ba0f1a59a760589
http://hdl.handle.net/11386/3124690
http://hdl.handle.net/11386/3124690
Publikováno v:
Rhinology. 34(3)
The Skin Prick Test (SPT) is the principal tool in allergic diagnosis, but in allergic rhinitisan immunological disease which affects 12% of the total population-the Nasal Provocation Test (NPT) allows more reliable results to be obtained. In our stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d116cbcfb83c1642c13536172b422296
https://pubmed.ncbi.nlm.nih.gov/8938885
https://pubmed.ncbi.nlm.nih.gov/8938885