Hugendubel.info - Die B2B Online-Buchhandlung 

Merkliste
Die Merkliste ist leer.
Bitte warten - die Druckansicht der Seite wird vorbereitet.
Der Druckdialog öffnet sich, sobald die Seite vollständig geladen wurde.
Sollte die Druckvorschau unvollständig sein, bitte schliessen und "Erneut drucken" wählen.
TaschenbuchKartoniert, Paperback
200 Seiten
Englisch
Wileyerschienen am01.06.2001
Brings together many of the main conclusions of the European Concerted Action Programme on Genetic Hearing Impairment (HEAR). This book is spilt into four sections, covering definitions, protocols, genotype/phenotype relationships and important websites.mehr

Produkt

KlappentextBrings together many of the main conclusions of the European Concerted Action Programme on Genetic Hearing Impairment (HEAR). This book is spilt into four sections, covering definitions, protocols, genotype/phenotype relationships and important websites.
Details
ISBN/GTIN978-1-86156-188-6
ProduktartTaschenbuch
EinbandartKartoniert, Paperback
FormatTrade Paperback (USA)
Verlag
Erscheinungsjahr2001
Erscheinungsdatum01.06.2001
Seiten200 Seiten
SpracheEnglisch
MasseBreite 156 mm, Höhe 234 mm, Dicke 11 mm
Gewicht313 g
Artikel-Nr.14563715
Rubriken
GenreMedizin

Inhalt/Kritik

Inhaltsverzeichnis
Introduction - putting together the pieces of the auditory puzzle Section 1 - Terminology and Definitions. Audiological terms. Vestibular definitions. Epidemiological terms. Genetic terms. Section 2 - Protocols. Audiometric investigation of probands. Audiometric investigation of first degree relatives. Audiometric investigation of carriers. Vestibular protocol. Epidemiological criteria. The European congenital ear anomaly inventory. Protocol for syndromal disorders associated with hearing impairment. How to collaborate with a genetic lab. Section 3 - Phenotype/Genotype Correlation. Introduction - Genotypes and phenotypes of non-syndromal hearing impairments. Phenotype/Genotype correlation autosomal dominant and autosomal recessive non-syndromatic hearing impairment. X-genotypes and phenotypes of non-syndromal X-linked hearing impairment. Phenotype/genotype correlation hearing impairment with mitochondrial DNA mutations. Section 4 - Relevant web sites. The hereditary hearing loss homepage. Connexin 26 (GJB2) deafness homepage.mehr

Autor

Alessandro Martini is the author of Definitions, Protocols and Guidelines in Genetic Hearing Impairment, published by Wiley. Manuela Mazzoli is the author of Definitions, Protocols and Guidelines in Genetic Hearing Impairment, published by Wiley.