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Klinische Gen-Analysen
- DEAFNESS, KID SYNDROME, BART-PUMPHREY SYNDROME
Analyse Details:
DEAFNESS, KID SYNDROME, BART-PUMPHREY SYNDROME
Testet das GJB2, GJB3, GJB6, GJA1, SLC26A4, SLC26A5, and Mitochondrial DNA Gen
 
Preis:
€ 720
DEAFNESS, KID SYNDROME, BART-PUMPHREY SYNDROME In die Einkaufsliste
 
DEAFNESS, KID SYNDROME, BART-PUMPHREY SYNDROME
Test-Details
GenGJB2, GJB3, GJB6, GJA1, SLC26A4, SLC26A5, and Mitochondrial DNA
OMIM
Tat-
MethodeDEAFNESS CHIP 200 positions
PrenatalNo
Order#PGWD0645
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