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- NIEDERLANDE
- Gelderland
- NIJMEGEN
- Molecular diagnosis in case of Multiple Congenital Anomalies (SNP-array)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
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- Molecular diagnosis of Kallmann syndrome heart disease (FGFR1 gene)
- Ospedali Galliera
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- SPANIEN
- Galicia
- SANTIAGO DE COMPOSTELA
- Molecular diagnosis of nonacquired pituitary hormone deficiency (PROP1, POU1F1, LHX4, HESX1 genes)
- CHUS - Complejo Hospitalario Universitario de Santiago
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- Molecular cytogenetic diagnosis of Kallmann syndrome
- Azienda Ospedaliera Universitaria Anna Meyer
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- Molecular cytogenetic diagnosis of Kallmann syndrome
- Azienda Ospedaliera Universitaria di Padova
- Mehr Informationen
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- Molecular diagnosis of mental retardation and autism by array-CGH
- Faculdade de Medicina da Universidade de Coimbra
- Mehr Informationen