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

Simple search

*
(*) mandatory field


 

6 Result(s)

Result(s)sorted by
Speciality(ies)/objective(s)
(6)
(3)
(1)
Technique(s)
(1)
(1)
Purpose(s)
(6)
Quality management
(3)
(5)
Country(ies)
(1)
(1)
(2)
(2)
RESET
Result(s)sorted by

Caption : Accreditation =Accreditation
;

    • Molecular diagnosis of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (CSF1R gene: sequencing)
    • Medizinisch Genetisches Zentrum München
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (CSF1R gene: sequencing)
    • CeGaT GmbH
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia (CSF1R gene / sequence analysis entire coding region)
    • Reference Laboratory Genetics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Accreditation
    • Molecular diagnosis of hereditary diffuse leukoencephalopathy with spheroids (CSF1R gene)
    • Praxis für Humangenetik
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia (CSF1R gene / entire coding sequence)
    • IMEGEN - Instituto de Medicina Genómica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia (CSF1R gene)
    • CHU de Nîmes - Hôpital Caremeau
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing
    • More information
    • FRANCE
    • LANGUEDOC-ROUSSILLON
    • NÎMES