Search for a diagnostic test
8 Result(s)
Laboratory officially designated for this diagnostic test
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Accreditation
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SWITZERLAND
Suisse Romande
GENÈVE
Search of duplications and/or deletions by array-CGH
Hôpitaux Universitaires de Genève HUG
Purpose(s)
: Antenatal diagnosis, Post-natal diagnosis
Specialty(ies)
: Molecular genetics, Cytogenetics
Service(s)
: Deletion / Duplication analysis, Detection of chromosome alterations large in size array based techniques, fish
GERMANY
Baden-Württemberg
TÜBINGEN
Diagnosis of genetic skeletal disorders (NGS Panel screening)
CeGaT GmbH
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Service(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis ngs sequencing (except wes)
GERMANY
Berlin
BERLIN
Diagnosis of bone and skeletal diseases (NGS Screening Panel: 408 genes)
Labor Berlin - Charité Vivantes GmbH
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Service(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis ngs sequencing (except wes), whole exome sequencing (wes)
FRANCE
AUVERGNE-RHONE-ALPES
CLERMONT-FERRAND
Diagnosis of rare genetic developmental defect during embryogenesis (Whole exome)
Centre de Biologie
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Service(s)
: Targeted mutation analysis, Sequence analysis: entire coding region sanger sequencing, whole exome sequencing (wes)
FRANCE
AUVERGNE-RHONE-ALPES
LYON
Diagnosis of developmental defects during embryogenesis (Whole exome)
Eurofins Biomnis
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Service(s)
: Sequence analysis: entire coding region whole exome sequencing (wes)
SWITZERLAND
Suisse Alémanique
BASEL
Diagnosis of developmental disorders by Twist Comprehensive Exome Panel
Universitätsspital Basel
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Service(s)
: Sequence analysis: entire coding region ngs sequencing (except wes), whole exome sequencing (wes)
SPAIN
Extremadura
BADAJOZ
Diagnosis of rare genetic developmental defect during embryogenesis
Hospital Universitario de Badajoz
Purpose(s)
: Antenatal diagnosis, Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Service(s)
: Sequence analysis: entire coding region, Deletion / Duplication analysis ngs sequencing (except wes), array based techniques, whole exome sequencing (wes)
GERMANY
Bayern
ERLANGEN