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SPAIN

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SABADELL

Diagnosis of Prader-Willi syndrome (SNRPN, SNORD116@ genes)
Corporación Sanitaria Parc Taulí
Purpose(s) : Antenatal diagnosis, Post-natal diagnosis
Specialty(ies) : Molecular genetics, Cytogenetics
Objective(s) : Uniparental disomy study, Methylation analysis, Deletion / Duplication analysis, Detection of microdeletions/microduplications
Technique(s) : MLPA based techniques, Array based techniques, FISH, Microsatellite analysis

POLAND

Warszawa
WARSAW

Molecular diagnostics of Prader-Willi syndrome (deletion, paternal disomy, imprinting defects at 15q11-13)
Instytut "Pomnik-Centrum Zdrowia Dziecka"
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Methylation analysis, Deletion / Duplication analysis
Technique(s) : MLPA based techniques

AUSTRIA

WIEN
WIEN

Molecular diagnosis of Prader-Willi syndrome (SALSA MS-MLPA probemix ME028-B2)
Medizinische Universität Wien
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics
Objective(s) : Methylation analysis, Deletion / Duplication analysis
Technique(s) : MLPA based techniques

SWEDEN

Stockholms läns landsting
STOCKHOLM

Molecular diagnosis of Prader Willi syndrome (PWCR gene)
Karolinska Universitetsjukhuset - Klinisk Genetik
Purpose(s) : Post-natal diagnosis
Specialty(ies) : Molecular genetics