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GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F05%3A00004106" target="_blank" >RIV/00216208:11130/05:00004106 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

  • Original language description

    GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

  • Czech name

    GJB2 mutace a stupeň ztráty sluchu: multricentrická studie

  • Czech description

    GJB2 mutace a stupeň ztráty sluchu: multricentrická studie

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FH - Neurology, neuro-surgery, nuero-sciences

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/NM7417" target="_blank" >NM7417: Mutation analysis of connexin 26 gene as the most frequent cause of prelingual nonsyndromic hearing loss.</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2005

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    American Journal of Human Genetics

  • ISSN

    0002-9297

  • e-ISSN

  • Volume of the periodical

    77

  • Issue of the periodical within the volume

    6

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    13

  • Pages from-to

    945-957

  • UT code for WoS article

  • EID of the result in the Scopus database