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Home
About us
Eurofins Genoma
Our team
Quality / Accreditation
Funded projects
Job opportunities
Our analyses
Useful Information
What a genetic test is
Where to get the test
How to request the test
How the genetic test is conducted
Sample collection and handling
Preservation and shipping of biological samples
Forms
Online reports
Where to find us
Contacts
IT
Category:
Otolaryngology
Congenital Deafness – Panel
Mitochondrial Nonsyndromic Hearing Loss and Deafness – MTRNR1 A1555G
Ashkenazi – Panel
Kallmann Syndrome, KAL1 (delXp22.31)
Joubert Syndrome – Panel
Usher Syndrome – Panel
Waardenburg Syndrome – Panel
Kallmann syndrome and Hypogonadotropic hypogonadism
GExome Clinical
GExome Proband
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