يعرض 1 - 3 نتائج من 3 نتيجة بحث عن '"Zenner, Hans-Peter"', وقت الاستعلام: 1.39s تنقيح النتائج
  1. 1
    دورية أكاديمية
    A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10.

    المؤلفون: Pfister M; Department of Otolaryngology, University of Tübingen, Tübingen, Germany., Tóth T, Thiele H, Haack B, Blin N, Zenner HP, Sziklai I, Nürnberg P, Kupka S

    المصدر: Molecular medicine (Cambridge, Mass.) [Mol Med] 2002 Oct; Vol. 8 (10), pp. 607-11.

    نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

    بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 9501023 Publication Model: Print Cited Medium: Print ISSN: 1076-1551 (Print) Linking ISSN: 10761551 NLM ISO Abbreviation: Mol Med Subsets: MEDLINE

    مواضيع طبية MeSH: Genetic Linkage/*genetics , Hearing Loss/*genetics , Mutagenesis, Insertional/*genetics , Trans-Activators/*genetics, Base Sequence ; Chromosome Mapping ; Female ; Frameshift Mutation/genetics ; Genotype ; Humans ; Hungary ; Male ; Molecular Sequence Data ; Pedigree ; Sequence Homology

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  2. 2
    دورية أكاديمية
    Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation.

    المؤلفون: Mirghomizadeh F; Hals-Nasen-Ohren-Klinik, Tübingen, Germany., Bardtke B, Devoto M, Pfister M, Oeken J, König E, Vitale E, Riccio A, De Rienzo A, Zenner HP, Blin N

    المصدر: European journal of human genetics : EJHG [Eur J Hum Genet] 2002 Feb; Vol. 10 (2), pp. 95-9.

    نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

    بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print Cited Medium: Print ISSN: 1018-4813 (Print) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

    مواضيع طبية MeSH: Genetic Linkage* , Proto-Oncogene Proteins c-bcl-2*, Carrier Proteins/*genetics , Chromosomes, Human, Pair 19/*genetics , Deafness/*genetics, Chromosome Mapping ; Genes, Dominant ; Humans ; Lod Score ; Myosin Heavy Chains ; Myosin Type II ; Pedigree ; Proto-Oncogene Proteins/genetics ; bcl-2-Associated X Protein

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  3. 3
    A 4bp-insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10

    المؤلفون: Pfister, Markus, Tóth, Tímea, Thiele, Holger, Haack, Birgit, Blin, Nikolaus, Zenner, Hans-Peter, Sziklai, István, Nürnberg, Peter, Kupka, Susan

    مصطلحات موضوعية: Male, Hungary, Base Sequence, Genotype, Genetic Linkage, Molecular Sequence Data, Chromosome Mapping, Sequence Homology, Orvostudományok, Klinikai orvostudományok, Pedigree, Mutagenesis, Insertional, Trans-Activators, Humans, Female, Frameshift Mutation, Hearing Loss, Research Article

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::2c8dc9ae592ff7a6fa5f782624c71f32

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