Skip to content
info@laboratoriogenoma.eu
| Contact center: +39 06 164 161 500
Facebook
Linkedin
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
Menu
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:
Array-CGH
Neuropathy Hereditary with Liability to Pressure Palsies HNPP (PMP22 – 17p12)
Kallmann Syndrome, KAL1 (delXp22.31)
Digeorge Syndrome (del22q11.2)
Angelman Syndrome (15q11.2-q13)
Charcot-Marie-Tooth Disease type 1A Demyelinating (PMP22 – dup17p12)
Wolf-Hirschhorn Syndrome (del4p16.3)
Sotos Syndrome (NSD1 – 5q35.2-q35.3)
Prader-Willi Syndrome (15q11.2)
Williams-Beuren Syndrome, WBS (7q11.23)
Molecular Karyotyping Array-CGH
←
older