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- Molecular diagnosis of Rolandic epilepsy with speech dyspraxia (SRPX2 gene: sequencing)
- Pränatalmedizin München
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- GERMANY
- Bayern
- REGENSBURG
- Molecular diagnosis of Rolandic epilepsy with speech dyspraxia (SRPX2 gene: sequencing, NGS panel polymicrogyria)
- Universitätsklinikum Regensburg
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- NETHERLANDS
- Gelderland
- NIJMEGEN
- Molecular diagnosis of X-linked Intellectual Deficit due to X-chromosome Inactivation (RFLP and methylation analysis of x-chromosome)
- Radboudumc - Radboud universitair medisch centrum
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- NETHERLANDS
- Utrecht
- UTRECHT
- Molecular diagnosis of X-linked Rolandic Epilepsy, Intellectual Deficit and Speech Dyspraxia (SRPX2 gene)
- UMC Utrecht - Universitair Medisch Centrum Utrecht
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- NETHERLANDS
- Utrecht
- UTRECHT
- Molecular diagnosis of Epileptic Encephalopathy (multigene panel; 32 genes)
- UMC Utrecht - Universitair Medisch Centrum Utrecht
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- NETHERLANDS
- Utrecht
- UTRECHT
- Molecular diagnosis of Focal Epilepsy (multigene panel; 9 genes)
- UMC Utrecht - Universitair Medisch Centrum Utrecht
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- GERMANY
- Mecklenburg-Vorpommern
- ROSTOCK
- Molecular diagnosis of Rolandic epilepsy with speech dyspraxia (SRPX2 gene)
- Centogene AG
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- GERMANY
- Baden-Württemberg
- TÜBINGEN
- Molecular diagnosis of Rolandic epilepsy with speech dyspraxia (SRPX2 gene: sequencing)
- CeGaT GmbH
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- SPAIN
- Comunidad Valenciana
- PATERNA
- Molecular diagnosis of rolandic epilepsy (SRPX2 gene)
- IMEGEN - Instituto de Medicina Genómica
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- Molecular diagnosis of rolandic epilepsy (SRPX2 gene)
- Azienda Ospedaliera Universitaria Senese - Ospedale Santa Maria alle Scotte
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