يعرض 1 - 2 نتائج من 2 نتيجة بحث عن '"IVS8 haplotyping"', وقت الاستعلام: 0.31s تنقيح النتائج
  1. 1
    Academic Journal
    Comprehensive and Rapid Genotyping of Mutations and Haplotypes in Congenital Bilateral Absence of the Vas Deferens and Other Cystic Fibrosis Transmembrane Conductance Regulator-Related Disorders ; Comprehensive and Rapid Genotyping of Mutations and Haplotypes in Congenital Bilateral Absence of the Vas Deferens and Other Cystic Fibrosis Transmembrane Conductance Regulator-Related Disorders: Improved Molecular Diagnosis of CBAVD

    المؤلفون: Bareil, Corinne, Guittard, Caroline, Altieri, Jean-Pierre, Templin, Carine, Claustres, Mireille, Des Georges, Marie

    المساهمون: Laboratoire de génétique des maladies rares. Pathologie moleculaire, etudes fonctionnelles et banque de données génétiques (LGMR), Université Montpellier 1 (UM1)-IFR3, Université Montpellier 1 (UM1)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)

    المصدر: ISSN: 1525-1578 ; Journal of Molecular Diagnostics ; https://www.hal.inserm.fr/inserm-00185153 ; Journal of Molecular Diagnostics, 2007, 9 (5), pp.582-588. ⟨10.2353/jmoldx.2007.070040⟩.

    مصطلحات موضوعية: CFTR, CBAVD, complete sequencing, IVS8 haplotyping, MESH: cystic fibrosis, MESH: cystic fibrosis transmembrane conductance regulator, [SDV.GEN]Life Sciences [q-bio]/Genetics, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics

    Relation: info:eu-repo/semantics/altIdentifier/pmid/17975025; inserm-00185153; https://www.hal.inserm.fr/inserm-00185153; https://www.hal.inserm.fr/inserm-00185153/document; https://www.hal.inserm.fr/inserm-00185153/file/Bareil_et_al.pdf; https://www.hal.inserm.fr/inserm-00185153/file/fig_Bareil_et_al.pdf; PUBMED: 17975025

    الاتاحة: https://www.hal.inserm.fr/inserm-00185153
    https://www.hal.inserm.fr/inserm-00185153/document
    https://www.hal.inserm.fr/inserm-00185153/file/Bareil_et_al.pdf
    https://www.hal.inserm.fr/inserm-00185153/file/fig_Bareil_et_al.pdf
    https://doi.org/10.2353/jmoldx.2007.070040

    View record in BASE

    أضف إلى المفضلة
  2. 2
    Comprehensive and Rapid Genotyping of Mutations and Haplotypes in Congenital Bilateral Absence of the Vas Deferens and Other Cystic Fibrosis Transmembrane Conductance Regulator-Related Disorders

    المؤلفون: Bareil, Corinne, Guittard, Caroline, Altieri, Jean-Pierre, Templin, Carine, Claustres, Mireille, Des Georges, Marie

    المساهمون: Laboratoire de génétique des maladies rares. Pathologie moleculaire, etudes fonctionnelles et banque de données génétiques (LGMR), Université Montpellier 1 (UM1)-IFR3, Université Montpellier 1 (UM1)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Bareil, Corinne

    المصدر: Journal of Molecular Diagnostics
    Journal of Molecular Diagnostics, American Society for Investigative Pathology (ASIP), 2007, 9 (5), pp.582-588. ⟨10.2353/jmoldx.2007.070040⟩

    مصطلحات موضوعية: [SDV.GEN]Life Sciences [q-bio]/Genetics, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, IVS8 haplotyping, CBAVD, [SDV.GEN] Life Sciences [q-bio]/Genetics, CFTR, complete sequencing, MESH: cystic fibrosis transmembrane conductance regulator, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, MESH: cystic fibrosis

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1398::0d7137e83892598dca5bc7d99aecbbc4
    https://www.hal.inserm.fr/inserm-00185153/document

    View record in OpenAIRE

    أضف إلى المفضلة
أدوات البحث: أحصل على تغذية RSS – أرسل هذا البحث بالبريد الإلكتروني – حفظ البحث – جدول التنبيهات: لا شيء