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Caption : Accreditation =Accreditation
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GERMANY

Thüringen
JENA

Accreditation
Molecular cytogenetic diagnosis of myeloproliferative disorders (PDGFRA and PDGFRB gene aberrations)
Institut für Humangenetik am Universitätsklinikum Jena
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics

UNITED KINGDOM

South Yorkshire
SHEFFIELD

Accreditation
Molecular monitoring of donor chimerism post stem cell transplantation
Sheffield Children's NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

GERMANY

Berlin
BERLIN

Accreditation
Molecular cytogenetic diagnosis of chronic myeloproliferative disease
Charité - Universitätsmedizin Berlin (CVK)
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

FRANCE

ILE-DE-FRANCE
SAINT-OUEN-L'AUMÔNE

Accreditation
Molecular diagnosis of hypereosinophilic syndrome (FIP1L1-PDGFRA fusion gene)
Laboratoire Cerba
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

GREECE

ATTIKI
ATHENS

Accreditation
Molecular and molecular cytogenetic diagnosis of hypereosinophilic syndrome (detection of FIP1L1-PDGFRA gene by FISH and RT-PCR)
BioAnalytica-GenoType SA
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Technique(s) : PCR based techniques, FISH

FRANCE

GRAND-EST
METZ

Accreditation
FISH diagnosis of hemopathies
CHR de Metz-Thionville
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technique(s) : FISH

GERMANY

Nordrhein-Westfalen
DORTMUND

Accreditation
Molecular diagnosis of chromosomal aberrations in AML, ALL, CML, AUL, CMML, MPN
Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics

UNITED KINGDOM

Avon
BRISTOL

Accreditation
Molecular diagnosis of Chronic myeloproliferative disease (MPL gene)
Southmead Hospital
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : PCR based techniques

SWITZERLAND

Suisse Romande
GENÈVE

Accreditation
Conventional (karyotype) and molecular cytogenetics (FISH) diagnosis of myeloproliferative neoplasm: diagnosis and prognosis
Hôpitaux Universitaires de Genève HUG
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

GERMANY

Bayern
MÜNCHEN

Accreditation
Molecular diagnosis of primary hypereosinophilic syndrome (PDGFRA gene)
Pränatalmedizin München
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
Technique(s) : Sanger sequencing, MLPA based techniques

NETHERLANDS

Noord-Holland
AMSTERDAM

Accreditation
Molecular diagnosis of Parkinson (gene panel)
VUmc - VU medisch centrum
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Sequence analysis: entire coding region
Technique(s) : Whole Exome Sequencing (WES)

AUSTRIA

OBERÖSTERREICH
LINZ

Accreditation
Molecular diagnosis of myoproliferative neoplasms (JAK2, CALR, MPL, CSF3R, SETBP1, ETNK1)
Krankenhaus der Barmherzigen Schwestern Linz
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : Sanger sequencing

AUSTRIA

OBERÖSTERREICH
LINZ

Accreditation
Molecular and molecular cytogenetic diagnosis of Hypereosinophilic syndrome (PDGFRbeta, FIP1L1-PDGFRalpha)
Krankenhaus der Barmherzigen Schwestern Linz
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Targeted mutation analysis, Detection of chromosome alterations large in size
Technique(s) : PCR based techniques, FISH

GERMANY

Bayern
MARTINSRIED

Accreditation
Molecular cytogenetic and cytogenetic diagnosis of chronic myeloproliferative disorders (translocations: t(3q26) [EVI1] deletions: 4q24 [TET2], 5q31 [EGR1] / 5q33-q34 [CSF1R], 7q22.1/7q31 [RELN/TES], 17p13 [TP53], 20q12 [MYBL2] numeric: -7 [RELN/TES], +8 [cen8], -Y [cen Y])
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

GERMANY

Bayern
MARTINSRIED

Accreditation
Molecular diagnosis of chronic myeloproliferative disorders (TET2 gene (exon 3-11), JAK2 gene (V617F), TP53 (exon 4-9))
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Objective(s) : Mutation scanning/screening and sequence analysis of selected exons
Technique(s) : Sanger sequencing

GERMANY

Schleswig-Holstein
KIEL

Accreditation
Molecular cytogenetic and cytogenetic diagnosis of hypereosinophilic syndromes (ETV6 (12p13), FGFR1 (8p12), FIP1L1/CHIC2/PDGFRA (4q12), PDGFRB (5q33))
Praxis Dr. Lana Harder
Purpose(s) : Post-natal diagnosis, Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

CANADA

Ontario
TORONTO

Accreditation
Molecular Diagnosis of Hypereosinophilic Syndrome (PDGFRA, FIP1L1 analysis)
Toronto General Hospital
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

FRANCE

ILE-DE-FRANCE
PARIS

Accreditation
Diagnosis of myeloproliferative neoplasm (Panel)
CHU Paris-GH St-Louis Lariboisière F.Widal - Hôpital Saint-Louis
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)

FRANCE

CENTRE-VAL DE LOIRE
CHAMBRAY-LES-TOURS

Accreditation
Diagnosis of hypereosinophilic syndrome (FIP1L1-PDGFRA fusion gene)
SELAS Arnaud-Biolys-Origet
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

FRANCE

OCCITANIE
MONTPELLIER

Cytogenetic diagnosis of malignant hemopathies
CHU de Montpellier - Hôpital Saint-Eloi
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics

TURKEY

TURKEY
ISTANBUL

Molecular diagnosis of myeloproliferative disorder with oesinophilia (PDGFRB gene)
Genetiks - Genetic diagnosis and research center
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

PORTUGAL

NORTE
PORTO

Molecular cytogenetic diagnosis of malignant haemopathies
Instituto Português de Oncologia do Porto, EPE / IPOFG - CRO Porto
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

SPAIN

Comunidad Valenciana
SANT JOAN D'ALACANT

Molecular cytogenetics diagnosis of hypereosinophilic syndromes (FISH FIP1L1/PDGFRA; PDGFRB)
Centro Inmunológico de Alicante (CIALAB)
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technique(s) : FISH

SPAIN

Asturias
OVIEDO

Molecular cytogenetic diagnosis of myeloproliferative neoplasm (FISH)
Hospital Universitario Central de Asturias
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics
Technique(s) : FISH

FRANCE

GRAND-EST
STRASBOURG

Cytogenetic diagnosis of myeloid hemopathies (classical caryotype and FISH)
CHU de Strasbourg - Hôpital de Hautepierre
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Technique(s) : FISH

FRANCE

BOURGOGNE-FRANCHE-COMTE
BESANÇON

Molecular cytogenetic diagnosis of malignant hemopathies
CHRU de Besançon - Hôpital Jean Minjoz
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Cytogenetics

FRANCE

OCCITANIE
TOULOUSE

Cytogenetic diagnosis of myeloid hemopathies
IUCT Oncopole - CLCC Institut Claudius Regaud
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH, Karyotyping

UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

Molecular and molecular cytogenetic diagnosis of Myeloproliferative neoplasm (BCR/ABL1, JAK2 (V617F and exon 12 mut), MPL (S505 and W515 mut), FIP1L1/PDGFRA
Cambridge University Hospitals NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics

UNITED KINGDOM

Cambridgeshire
CAMBRIDGE

KIT (D816V): Molecular diagnosis of Chronic Myeloid Leukaemia (BCR/ABL1: by PCR, RT-PCR and FISH)
Cambridge University Hospitals NHS Foundation Trust
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics, Cytogenetics
Technique(s) : PCR based techniques, FISH

ITALY

LOMBARDIA
VARESE

Molecular diagnosis of myeloproliferative neoplasm (JAK2 gene)
A.O.U. Ospedale di Circolo e Fondazione Macchi - Università dell'Insubria
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Targeted mutation analysis
Technique(s) : NGS sequencing (except WES)

CZECH REPUBLIC

South Moravia
BRNO

Molecular diagnosis of hypereosinophilic syndrome (FIP1L1/PDGFRA fusion gene)
University hospital Brno
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

SPAIN

Canarias
SANTA CRUZ DE TENERIFE

Diagnosis of hypereosinophilic syndrome
Hospital Universitario de Canarias
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size
Technique(s) : FISH

GREECE

LARISA
LARISSA

Molecular diagnosis of hypereosinophilic syndrome (FIP1L1-PDGFRA fusion gene: RT-PCR, nested PCR and sequencing analyses)
University of Thessaly (UTH)
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics
Technique(s) : PCR based techniques

CZECH REPUBLIC

Moravia-Silesia
OSTRAVA

Molecular diagnosis of hypereosinophilic syndrome (PDGFRA gene)
CGB laboratory Ltd.
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

LITHUANIA

DZUKIJA
VILNIUS

Molecular diagnosis of hypereosinophilic syndromes (FIP1L1-PDGFRA fusion gene)
Vilnius University Hospital Santariskiu Klinikos
Purpose(s) : Somatic genetics
Specialty(ies) : Molecular genetics

SPAIN

Madrid
SAN SEBASTIÁN DE LOS REYES

Diagnosis of hypereosinophilic syndrome (ETV6, FGFR1, FIP1L1, PDGFRA, PDGFRB genes)
Laboratorio de Genética Clínica, S.L.
Purpose(s) : Antenatal diagnosis, 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
Technique(s) : Sanger sequencing

AUSTRIA

WIEN
WIEN

Molecular cytogenetic diagnosis of myeloproliferative neoplasms (t(9;22)(q34;q11); BCR-ABL amplification, +8, +9, +21, -5/5q-, -7/7q-, 20q-, 13q-, 12p-, i(17q), CHIC2-deletion (FIP1L1/PDGFRa rearrangement), rearrangements of PDGFRa, -b, FGFR1; further analyses upon request)
Labordiagnostik GmbH
Purpose(s) : Somatic genetics
Specialty(ies) : Cytogenetics
Objective(s) : Detection of chromosome alterations large in size, Detection of microdeletions/microduplications
Technique(s) : M-FISH/SKY, FISH