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Klinische Gen-Analysen
- USHER SYNDROME and NON-SYNDROMIC DEAFNESS
Analyse Details:
USHER SYNDROME and NON-SYNDROMIC DEAFNESS
Testet das USHER TYPE 1: MYO7A encoding Myosin 7A for Usher syndrome type 1A/B (USH1A/B), USH1C encoding Harmonin for Usher syndrome type 1C (USH1C), CDH23 encoding Cadherin23 for Usher syndrome type 1D (USH1D), PCDH15 encoding Protocadherin15 for Usher syndrome typ Gen
 
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USHER SYNDROME and NON-SYNDROMIC DEAFNESS In die Einkaufsliste
 
USHER SYNDROME and NON-SYNDROMIC DEAFNESS
Test-Details
GenUSHER TYPE 1: MYO7A encoding Myosin 7A for Usher syndrome type 1A/B (USH1A/B), USH1C encoding Harmonin for Usher syndrome type 1C (USH1C), CDH23 encoding Cadherin23 for Usher syndrome type 1D (USH1D), PCDH15 encoding Protocadherin15 for Usher syndrome typ
OMIM
Tat-
Methode19 genes
PrenatalNo
Order#PGWD2185
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