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Eurofins Genoma
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Home
About us
Eurofins Genoma
Our Team
Quality/Accreditation
Funded Projects
Job Opportunities
Specialized Areas
Useful information
What is a genetic test
Where you can test
How to request the test
How the genetic test is performed
Sample collection and management
Storage and shipment of biological samples
Forms
Online Reports
Contacts
ENG
ITA
Category:
Neurology
Opitz G/BBB Syndrome – Panel
Legius Syndrome
Parkinson Disease – Expanded Panel
Prader Willi/Angelman Syndromes – Panel
Amyotrophic Lateral Sclerosis (ALS) and frontotemporal dementia – Panel
X Fragile FRAXA/FRAXE
Myotonic Dystrophy Type 1, Steinert Disease
FGFR3 G380R
Hypochondroplasia – FGFR3 Gene Mutations
Androgen Receptor AR – NGS Gene Sequencing
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