Search for a diagnostic test
24 Result(s)
Caption
: Accreditation
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GERMANY
Nordrhein-Westfalen
DORTMUND
Molecular diagnosis of multiple endocrine neoplasia type 1 (MEN1 gene)
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

GERMANY
Bayern
MÜNCHEN
Molecular diagnosis of intestinal carcinoid tumors (SDHD gene)
Pränatalmedizin München
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: Sanger sequencing

FRANCE
PAYS DE LA LOIRE
ANGERS
Diagnosis of tumors (Panel)
CHU d'Angers
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

FRANCE
HAUTS-DE-FRANCE
LILLE
Diagnosis of endocrine diseases (Panel)
CHRU de Lille - Centre de Biologie Pathologie Génétique
Purpose(s)
: Post-natal diagnosis, Pre-symptomatic diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, PCR based techniques, MLPA based techniques

FRANCE
OCCITANIE
TOULOUSE
Diagnosis of endocrine tumors (Panel)
CHU de Toulouse - Hôpital Purpan
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons
Technique(s)
: NGS sequencing (except WES)

GERMANY
Bayern
MÜNCHEN
Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Medizinisch Genetisches Zentrum München
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

GERMANY
Baden-Württemberg
ULM
Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universitätsklinikum Ulm
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

GERMANY
Bayern
WÜRZBURG
Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universität Würzburg - Biozentrum
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

FRANCE
PROVENCE-ALPES-COTE D'AZUR
MARSEILLE
Diagnosis of familial isolated digestive endocrine tumors (Panel)
CHU de Marseille - Hôpital de la Conception
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis, Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s)
: NGS sequencing (except WES), Sanger sequencing, MLPA based techniques

SPAIN
País Vasco
SAN SEBASTIÁN
Molecular diagnosis of endocrine tumor (TMEM127, SDHD, SHCD, CDC73, SDHB, SDHAF2, VHL, MEN1, AIP genes / array-CGH)
Policlínica Gipuzkoa
Purpose(s)
: Post-natal diagnosis, Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Deletion / Duplication analysis
Technique(s)
: Array based techniques

SPAIN
País Vasco
BARAKALDO
Molecular diagnosis of Zollinger-Ellison syndrome (MEN1 gene)
Hospital Universitario Cruces - Osakidetza
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics

FRANCE
ILE-DE-FRANCE
PARIS
Diagnosis of endocrine diseases (Panel)
CHU Paris Centre - Hôpital Cochin
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons
Technique(s)
: NGS sequencing (except WES)

GERMANY
Sachsen
DRESDEN
Molecular diagnosis of cancers predisposition by TruSight Cancer panel (NGS panel)
Universitätsklinikum Carl Gustav Carus an der TU Dresden
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Molecular genetics
Objective(s)
: Sequence analysis: entire coding region
Technique(s)
: NGS sequencing (except WES)

FRANCE
NORMANDIE
ROUEN
Histological and immunohistological of neuroendocrine tumor of the pancreas and digestive tube
CHU de Rouen - Hôpital Charles Nicolle
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Biochemical genetics, Pathology
Objective(s)
: Protein expression
Technique(s)
: Immunohistochemistry

GERMANY
Thüringen
BAD BERKA
Nuclear medicine diagnosis of neuroendocrine tumors (gallium-68 somatostatin Receptor-PET/CT)
Zentralklinik Bad Berka GmbH
Purpose(s)
: Post-natal diagnosis
Specialty(ies)
: Imaging

CYPRUS
Cyprus
NICOSIA
Mutation screening of gastrointestinal cancer syndromes (C-KIT 4q12)
The Cyprus Institute of Neurology and Genetics
Purpose(s)
: Post-natal diagnosis, Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons

CYPRUS
Cyprus
NICOSIA
Analysis of known mutations for gastrointestinal cancer (C-KIT 4q12)
The Cyprus Institute of Neurology and Genetics
Purpose(s)
: Post-natal diagnosis, Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis

CYPRUS
Cyprus
NICOSIA
Analysis of known mutations for gastrointestinal cancer (PDFGRA 4q12)
The Cyprus Institute of Neurology and Genetics
Purpose(s)
: Post-natal diagnosis, Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis

CYPRUS
Cyprus
NICOSIA
Mutation screening for gastrointestinal cancer (PDFGRA 4q12)
The Cyprus Institute of Neurology and Genetics
Purpose(s)
: Post-natal diagnosis, Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons

CYPRUS
Cyprus
NICOSIA
Mutation screening for gastrointestinal cancer (CDH1 16q22.1)
The Cyprus Institute of Neurology and Genetics
Purpose(s)
: Post-natal diagnosis, Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons

CYPRUS
Cyprus
NICOSIA
Analysis of known mutations for gastrointestinal cancer (CDH1 16q22.1)
The Cyprus Institute of Neurology and Genetics
Purpose(s)
: Post-natal diagnosis, Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis

CYPRUS
Cyprus
NICOSIA
Analysis of known mutations for gastrointestinal cancer (VHL 3p25.3)
The Cyprus Institute of Neurology and Genetics
Purpose(s)
: Post-natal diagnosis, Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Targeted mutation analysis

CYPRUS
Cyprus
NICOSIA
Mutation screening for gastrointestinal cancer (VHL 3p25.3)
The Cyprus Institute of Neurology and Genetics
Purpose(s)
: Post-natal diagnosis, Somatic genetics
Specialty(ies)
: Molecular genetics
Objective(s)
: Mutation scanning/screening and sequence analysis of selected exons

FRANCE
CENTRE-VAL DE LOIRE
TOURS