Skip to
  1. Homepage
  2. Diagnostic tests
  3. Search
Simple search

Simple search

*
(*) mandatory field




 

Other search option(s)

14 matching term(s)

Result(s)sorted by

Caption : Accreditation =Accreditation
;

    • NETHERLANDS
    • Zuid-Holland
    • LEIDEN
    • Accreditation
    • Molecular diagnosis of Hereditary Cerebral Hemorrhage with Amyloidosis (APP gene)
    • LUMC - Leids Universitair Medisch Centrum
    • More information
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Accreditation
    • Molecular diagnosis of hereditary cerebral hemorrhage with amyloidosis, Icelandic type (CST3 gene)
    • Reference Laboratory Genetics
    • More information
    • FRANCE
    • HAUTE-NORMANDIE
    • ROUEN
    • Molecular diagnosis of hereditary cerebral hemorrhages with amyloidosis (APP gene)
    • Faculté de médecine et de pharmacie de Rouen
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of cerebral amyloid angiopathies (APP, TTR and gelsolin genes)
    • CHU Paris-GH St-Louis Lariboisière F-Widal - Hôpital Lariboisière
    • More information
    • BELGIUM
    • ANTWERPEN
    • ANTWERPEN
    • Molecular diagnosis of Cerebral amyloid angiopathy (APP gene, APP promotor, APP duplication)
    • University of Antwerp - UA
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Cerebral amyloid angiopathy (CST3 and ITM2B genes: sequencing of the entire coding region)
    • CGC Genetics / Centro de Genética Clínica
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of hereditary cerebral hemorrhage with amyloidosis (APP, CST3 genes / entire coding sequence)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of hereditary cerebral hemorrhage with amyloidosis (duplications of APP gene by MLPA analysis and entire coding sequence / exons 16 and 17)
    • Lorgen G.P.
    • More information
    • DENMARK
    • Sjælland
    • COPENHAGEN
    • Molecular diagnosis of familial amyloidosis
    • Statens Serum Institut
    • More information
    • GERMANY
    • Schleswig-Holstein
    • KIEL
    • Histological diagnosis of amyloidosis
    • Universitätsklinikum Schleswig-Holstein - Campus Kiel
    • More information
    • GERMANY
    • Hamburg
    • HAMBURG
    • Histological and cytological diagnosis of amyloidosis
    • Kath. Marienkrankenhaus gGmbH
    • More information
    • GERMANY
    • Bayern
    • MARTINSRIED
    • Histological diagnosis and immunohistochemical classification of amyloidosis
    • Innovationszentrum für Biotechnology (IZB)
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of hereditary cerebral hemorrhage with amyloidosis (entire coding sequence of APP gene and exons 16 and 17 / duplications by MLPA analysis)
    • Laboratorio de Genética Clínica, S.L.
    • More information
    • DENMARK
    • Jylland
    • AARHUS
    • Molecular diagnosis of amyloidosis
    • Aarhus Universitetshospital - Skejby
    • More information