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- Molecular diagnosis of holoprosencephaly (GLI2, SHH, SIX3, TGIF and ZIC2 genes)
- Medizinische Genetik Dresden
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- GERMANY
- Baden-Württemberg
- MANNHEIM
- Molecular diagnosis of Holoprosencephaly 7 (PTCH1 gene)
- Zentrum für Humangenetik Mannheim
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- GERMANY
- Bayern
- REGENSBURG
- Molecular diagnosis of holoprosencephaly (GLI2, NODAL, PTCH1, SHH, SIX3, TGIF, ZIC2 genes: sequencing / MLPA)
- Universitätsklinikum Regensburg
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- NETHERLANDS
- Limburg
- MAASTRICHT
- Molecular diagnosis of Holoprosencephaly (SIX3, ZIC2, TGIF, SHH, GLI2, DISP1 and PTCH1 gene)
- AZM - Academisch Ziekenhuis Maastricht
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- NETHERLANDS
- Gelderland
- NIJMEGEN
- Molecular diagnosis in case of Unexplained Intellectual Deficit (SNP-array)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
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- NETHERLANDS
- Gelderland
- NIJMEGEN
- Molecular diagnosis in case of Multiple Congenital Anomalies (SNP-array)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
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- NETHERLANDS
- Gelderland
- NIJMEGEN
- Molecular diagnosis in case of Unexplained Intellectual Deficit (exome sequencing)
- UMC St Radboud - Universitair Medisch Centrum St Radboud
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- GERMANY
- Baden-Württemberg
- FREIBURG
- Molecular diagnosis of Holoprosencephaly 7 (PTCH1 gene)
- Praxis für Humangenetik / Center for Human Genetics Freiburg
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- UNITED KINGDOM
- Wiltshire
- SALISBURY
- Molecular Cytogenetic diagnosis of Holoprosencephaly (by FISH of SIX3)
- Salisbury District Hospital
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- GERMANY
- Hessen
- FRANKFURT AM MAIN
- Molecular diagnosis of holoprosencephaly 2 and 7 (PTCH1, SIX3 genes)
- Zentrum für Humangenetik
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- GERMANY
- Baden-Württemberg
- TÜBINGEN
- Molecular diagnosis of holoprosencephaly (PTCH1, SHH, ZIC2 genes: sequencing)
- CeGaT GmbH
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- Molecular diagnosis of holoprosencephaly (PTCH1, GAS1, GLI2, SHH, ZIC2, SIX3 and TGIF genes)
- CHU de Rennes - Hôpital Pontchaillou
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- FRANCE
- HAUTE-NORMANDIE
- ROUEN
- Molecular cytogenetic diagnosis of holoprosencephaly (SHH gene deletion)
- CHU de Rouen - Hôpital Charles Nicolle
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- Molecular diagnosis of holoprosencephaly (SHH gene)
- IRCCS Istituto G. Gaslini - Ospedale Pediatrico
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- GERMANY
- Baden-Württemberg
- FREIBURG
- Molecular diagnosis of holoprosencephaly 2 and 3 (SIX3, SHH genes)
- Universitätsklinikum Freiburg
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- SPAIN
- Galicia
- SANTIAGO DE COMPOSTELA
- Molecular diagnosis of holoprosencephaly (SHH, SIX3, TGIF1 and ZIC2 genes)
- CHUS - Complejo Hospitalario Universitario de Santiago
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- SPAIN
- 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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- SPAIN
- País Vasco
- SAN SEBASTIÁN
- Molecular diagnosis of holoprosencephaly (array-CGH)
- Policlínica Gipúzcoa
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- SPAIN
- Comunidad Valenciana
- PATERNA
- Molecular diagnosis of holoprosencephaly (SHH gene)
- Sistemas Genómicos S.L.
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- GERMANY
- Niedersachsen
- OSNABRÜCK
- Molecular diagnosis of holoprosencephaly (SHH, SIX3, ZIC2 genes)
- Praxis Dres. Gencik
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- Molecular diagnosis of holoprosencephaly (PTCH1, SHH, ZIC2, SIX3, TGIF1 genes)
- Fundación Jiménez Díaz
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- Molecular diagnosis of Holoprosencephaly (SHH, TGIF, and ZIC2 genes)
- Praxis für Humangenetik
- More information
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- Molecular diagnosis of holoprosencephaly (SHH gene)
- Oslo University Hospital, Ullevaal
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- Molecular cytogenetic diagnosis of holoprosencephaly (HPE1, HPE3, HPE4, HPE6)
- Universitätsklinikum Carl Gustav Carus an der TU Dresden
- More information
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- GERMANY
- Nordrhein-Westfalen
- BONN
- Molecular diagnosis of holoprosencephaly 3 (SHH gene)
- Institut für Klinische Genetik Bonn
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- GERMANY
- Baden-Württemberg
- STUTTGART
- Molecular diagnosis of Holoprosencephaly 7 (PTCH1 gene: sequencing / MLPA)
- Praxis für Humangenetik und Prävention
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- SPAIN
- Comunidad Valenciana
- PATERNA
- Molecular diagnosis of holoprosencephaly (SHH gene - entire coding sequence)
- IMEGEN - Instituto de Medicina Genómica
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- Molecular diagnosis of Holoprosencephaly 7 (PTCH1 gene: sequencing)
- Gemeinschaftspraxis für Humangenetik
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- FRANCE
- NORD-PAS-DE-CALAIS
- LILLE
- Molecular cytogenetics diagnosis of holoprosencephaly : search for microdeletions in HPE1 and HPE6 locus and in SIX3, SHH, TGIF, ZIC2 and PTCH1 genes
- Hopital Saint Vincent de Paul
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- Molecular diagnosis of multiple congenital pituitary deficiency
- Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
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- Biochemical diagnosis of nonacquired combined pituitary hormone deficiency
- Hospital de la Santa Creu i Sant Pau
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- SPAIN
- Madrid
- SAN SEBASTIÁN DE LOS REYES
- Molecular diagnosis of holoprosencephaly (deletions by MLPA analysis and entire coding sequence of SHH, ZIC2, SIX3 and TGIF1 genes)
- LABORATORIO DE GENÉTICA CLÍNICA S.L.
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- Molecular diagnosis of holoprosencephaly (aCGH)
- Genetadi Biotech S.L.
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