NL
FGA - Dysfibrinogenemia
This test is available for the following conditions:
- Conditions > Hematological, hereditary > Fibrinogenemia (a-, hypo-, dys-)
This product is also part of the following panels:
- WES comprehensive preconception carrier test ¹
- WES hemostatic/thrombotic disorders (100.0% *)
- WES Mendelian inherited disorders (100.0% *)
* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
134820
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
FGB - Dysfibrinogenemia
This test is available for the following conditions:
- Conditions > Hematological, hereditary > Fibrinogenemia (a-, hypo-, dys-)
This product is also part of the following panels:
- WES comprehensive preconception carrier test ¹
- WES hemostatic/thrombotic disorders (100.0% *)
- WES Mendelian inherited disorders (100.0% *)
* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
134830
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
FGG - Dysfibrinogenemia
This test is available for the following conditions:
- Conditions > Hematological, hereditary > Fibrinogenemia (a-, hypo-, dys-)
This product is also part of the following panels:
- WES comprehensive preconception carrier test ¹
- WES hemostatic/thrombotic disorders (100.0% *)
- WES Mendelian inherited disorders (100.0% *)
* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
134850
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane
