genetische test
|
moleculair genetisch onderzoek (verrichting)
moleculair genetisch onderzoek
moleculaire genetische test
Molecular genetic test
Id
405825005
Status
primitief
methode
evaluatie
Global Patient Set
DHD Verrichtingenthesaurus-referentieset
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BRCA1 mutation carrier detection test
BRCA2 mutation carrier detection test
Cystic fibrosis 20 common mutation test
Cystic fibrosis 29 common mutation test
detecteren van gen voor humane epidermale groeifactorreceptor 2
3
Detection of Arg3527Gln mutation in apolipoprotein B-100 gene
Detection of BCR-ABL translocation
Detection of factor V Leiden mutation and prothrombin G20210A mutation
Detection of mutation in apolipoprotein B-100 gene
Detection of mutation in low density lipoprotein receptor gene
Factor II (prothrombin) G20210A mutation detection
Factor VIII mutation carrier detection test
Familial medullary thyroid carcinoma mutation carrier detection test
genmutatieanalyse
2
genprofieltest voor borstkanker
Huntington disease gene mutation carrier detection test
moleculair genetisch onderzoek naar 'copy number variations' van genoom
moleculair genetisch onderzoek naar 'regions of homozygosity' van genoom
moleculair genetisch onderzoek naar pathogene mutaties in exoom
Multiple endocrine neoplasia type 2A mutation carrier detection test
Multiple endocrine neoplasia type 2B mutation carrier detection test
Neurofibromatosis type 1 mutation carrier detection test
Neurofibromatosis type 2 mutation carrier detection test
onderzoek naar dragerschap van gendefect
Quantitation of BCR-ABL translocation
Targeted analysis for gene mutation
Testing for known gene mutation in family member
2
Von Hippel-Lindau disease mutation carrier detection test
