Paolo Gasparini - European Medicines Agency - Europa
www.ema.europa.eu
Rachel E.Bell, Salvatore Melchionda, Leopoldo Zelante, Karen B. Avraham, Paolo Gasparini. Multiple mutations of MYO1A, a Cochlear-Expressed gene, ...
A novel missense mutation in the Connexin DOKUMEN.TIPSdokumen.tips › Documents
dokumen.tips
... Rosamaria Santarelli b,Massimo Carella a, Leopoldo Zelante a, Luisa Toffolatti c,Teresa Palladino a, Salvatore Melchionda a, Edoardo Arslan b.
A novel missense mutation in the Connexin FDOCUMENTSfdocuments.net › Documents
fdocuments.net
Oct 15, · ... Santarelli b,Massimo Carella a, Leopoldo Zelante a, Luisa Toffolatti c,Teresa Palladino a, Salvatore Melchionda a, Edoardo Arslan b.
[PDF] Landmark3910.pdf - IMR Pressarticle.imrpress.com › bri › Landmark › articles › pdf › Landmark3910
article.imrpress.com
Bicego, Salvatore Melchionda, Leopoldo Zelante, Enzo. Di Iorio, Roberto Bruzzone, Paolo Gasparini: Hearing loss: frequency and functional studies of the ...
CiteSeerX
citeseerx.ist.psu.edu
BibTeX @MISC{Zelante97, author = {Leopoldo Zelante and Paolo Gasparini and Xavier Estivill and Salvatore Melchionda and Nancy Govea and Monserrat Milá and Matteo Della Monica and Jaber Lutfi and Mordechai Shohat and Elaine Mansfield and Kathleen Delgrosso and Saul Surrey and Paolo Fortina}, title = {}, year = {1997}}
Are MYO1C and MYO1F associated with hearing loss? - ScienceDirect
www.sciencedirect.com
Cristina Zadro,; Maria Stella Alemanno,; Emanuele Bellacchio,; Romina Ficarella, ; Francesca Donaudy,; Salvatore Melchionda,; Leopoldo Zelante,; Raquel ...
Multiple Mutations of MYO1A, a Cochlear-Expressed Gene, in...
www.ncbi.nlm.nih.gov
Francesca Donaudy, 1 Antonella Ferrara, 2 Laura Esposito, 1 Ronna Hertzano, 3 Orit Ben-David, 3 Rachel E. Bell, 4 Salvatore Melchionda, 5 Leopoldo Zelante, 5 Karen B
Pathogenetic role of the deafness-related M34T mutation of Cx26
www.ncbi.nlm.nih.gov
Massimiliano Bicego, 1 † Martina Beltramello, 2 † Salvatore Melchionda, 3 Massimo Carella, 3 Valeria Piazza, 2 Leopoldo Zelante, 3 Feliksas F. Bukauskas, 4
- CORE
core.ac.uk
By Leopoldo Zelante, Paolo Gasparini, Xavier Estivill, Salvatore Melchionda, Nancy Govea, Monserrat Milá, Matteo Della Monica, Jaber Lutfi, Mordechai Shohat, Elaine Mansfield, Kathleen Delgrosso, Saul Surrey and Paolo Fortina
Report Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Core
core.ac.uk
Carsten M. Pusch,6 Peter Nu¨rnberg,7,8 Salvatore Melchionda,9 Leopoldo Zelante,9. Ester Ballana,10 Xavier Estivill,10 Guy Van Camp,3 ...
nature.com search
www.nature.com
Salvatore Melchionda, Marco Seri, Massimo Carella, Maria Rosaria Piemontese, Xiao-xiao Zhang, Leopoldo Zelante, Giovanni Romeo & Paolo Gasparini.
All web results to the name "Salvatore Melchionda"
CURRICULUMVITAE (Formativo e Professionale - studylibit.comstudylibit.com › Scienza › Biologia › Biochimica › Genetica
studylibit.com
Paolo Gasparini, Salvatore Melchionda, Enzo Di Iorio, Anna Grifa, Leopoldo Zelante. “Sordità” su Malattie Genetiche Molecole e Geni , A Cao, ...
Ficarella, Romina: free download. Ebooks library. On-line books ...booksc.siteunblock.pw › ...
booksc.siteunblock.pw
Cristina Zadro, Maria Stella Alemanno, Emanuele Bellacchio, Romina Ficarella, sca Donaudy, Salvatore Melchionda, Leopoldo Zelante, Raquel Rabionet, ...
Molecular basis of childhood deafness resulting from mutations in ...www.academia.edu › Molecular_basis_of_childhood_deafness_resulting_fr...
www.academia.edu
... O R I G I N A L I N V E S T I G AT I O N Raquel Rabionet · Leopoldo Zelante · Núria López-Bigas · Leonardo D'Agruma · Salvatore Melchionda · Gabriella ...
Functional characterization of a novel Cx26 (T55N) mutation...
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Salvatore Melchionda, Massimiliano Bicego, Elio Marciano, Annamaria Franzè, Marcello Morgutti, Grazia Bortone, Leopoldo Zelante, Massimo Carella, Paola D' ...
Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6...
moh-it.pure.elsevier.com
Elona Cama, Salvatore Melchionda, Teresa Palladino, Massimo Carella, Rosamaria Santarelli, Elisabetta Genovese, Filippo Benettazzo, Leopoldo Zelante, ...
Connexin26 Mutations Associated with the Most Common Form of...
oxfordindex.oup.com
Leopoldo Zelante, Paolo Gasparini, Xavier Estivill, Salvatore Melchionda, Leonardo D'Agruma, Nancy Govea, Monserrat Milá, Matteo Della Monica, Jaber Lutfi, ...
WikiGenes -
www.wikigenes.org
Elona Cama, Salvatore Melchionda, Teresa Palladino, Massimo Carella, Rosamaria Santarelli, Elisabetta Genovese, Filippo Benettazzo, Leopoldo Zelante, ...
Papers with the keyword Expanded newborn screening (Page ...read.qxmd.com › keyword
read.qxmd.com
Salvatore Melchionda, Teresa Palladino, Stefano Castellana, Mario Giordano, Elisa Benetti, Patrizia De Bonis, Leopoldo Zelante, Luigi Bisceglia. Autosomal ...
Molecular basis of childhood deafness resulting from mutations in the...
moh-it.pure.elsevier.com
Raquel Rabionet ; Leopoldo Zelante ; Núria López-Bigas ; Leonardo D'Agruma ; Salvatore Melchionda ; Gabriella Restagno ; Maria Lourdes Arbonés ; Paolo ...
Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and...
www.infona.pl
... Declau Carsten M. Pusch Peter Nürnberg Salvatore Melchionda Leopoldo Zelante Ester Ballana Xavier Estivill Guy Van Camp Paolo Gasparini Anna Savoia.
Related search requests for Salvatore Melchionda
| Giovanni Rotondo Bruno Dallapiccola Teresa Palladino | Elisabetta Genovese Xavier Estivill Edoardo Arslan | Michael Petersen Anna Grifa Paolo Fortina |
People Forename "Salvatore" (9420) Name "Melchionda" (29) |
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