Centrum Medische Genetica - UZ Gent

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Name of the laboratory:
Centrum Medische Genetica - UZ Gent
Abbreviation:
UGent
RIZIV number:
84499074-996
Address:

C. Heymanslaan, 10
9000 Gent
East Flanders
Belgium

Telephone:
Fax:
E-mail:
info.cmgg@uzgent.be
URL:
EQA:
2019 DNA Sequencing – NGS (vGermline) EMQN
2020 DNA Sequencing – NGS (vGermline) EMQN
2021 DNA Sequencing – NGS (vGermline) EMQN
2022 DNA Sequencing – NGS (vGermline) EMQN
2023 DNA Sequencing – NGS (vGermline) EMQN
2019 DNA Sequencing - Sanger EMQN
2020 DNA Sequencing - Sanger EMQN
2021 DNA Sequencing - Sanger EMQN
2022 DNA Sequencing - Sanger EMQN
2023 DNA Sequencing - Sanger EMQN
2019 Postnatal constitutional CNV detection (array) GenQA (Genomics Quality Assessment)
2020 Postnatal constitutional CNV detection EMQN
2021 Postnatal constitutional CNV detection EMQN
2022 Postnatal constitutional CNV detection GenQA (Genomics Quality Assessment)
2023 Postnatal constitutional CNV detection GenQA (Genomics Quality Assessment)
2020 Prenatal constitutional CNV detection GenQA (Genomics Quality Assessment)
2021 Prenatal constitutional CNV detection GenQA (Genomics Quality Assessment)
2022 Prenatal constitutional CNV detection GenQA (Genomics Quality Assessment)
2023 Prenatal constitutional CNV detection GenQA (Genomics Quality Assessment)
2019 Blood -postnatal GenQA (Genomics Quality Assessment)
2020 Blood postnatal GenQA (Genomics Quality Assessment)
2021 Recurrent miscarriage karyotyping GenQA (Genomics Quality Assessment)
2021 Sex chromosome disorders karyotyping GenQA (Genomics Quality Assessment)
2022 Postnatal karyotyping GenQA (Genomics Quality Assessment)
2019 Pathogenicity of sequence variants GenQA (Genomics Quality Assessment)
2021 Pathogenicity of germline sequence variant GenQA (Genomics Quality Assessment)
2021 Pathogenicity of germline postnatal copy number variants (CNV) (Classification only) GenQA (Genomics Quality Assessment)
2019 PGT for monogenic disorders GenQA (Genomics Quality Assessment)
2020 PGT for monogenic disorders GenQA (Genomics Quality Assessment)
2021 PGT for monogenic disorders GenQA (Genomics Quality Assessment)
2022 PGT for monogenic disorders GenQA (Genomics Quality Assessment)
2023 PGT for monogenic disorders GenQA (Genomics Quality Assessment)
2020 PGT for chromosomal rearrangements (NGS/arrays) GenQA (Genomics Quality Assessment)
2022 PGT for chromosomal rearrangements (NGS/arrays) GenQA (Genomics Quality Assessment)
2019 PGT for common aneuploidies GenQA (Genomics Quality Assessment)
2021 PGT for common aneuploidies GenQA (Genomics Quality Assessment)
2023 PGT for common aneuploidies GenQA (Genomics Quality Assessment)
2021 ISCN (classification only) GenQA (Genomics Quality Assessment)
2022 ISCN (classification only) GenQA (Genomics Quality Assessment)
2023 ISCN (classification only) GenQA (Genomics Quality Assessment)
2020 Pregnancy loss GenQA (Genomics Quality Assessment)
2021 Pregnancy loss GenQA (Genomics Quality Assessment)
2023 Pregnancy loss GenQA (Genomics Quality Assessment)
2022 NIPT for common aneuploidies GenQA (Genomics Quality Assessment)
2023 NIPT for common aneuploidies GenQA (Genomics Quality Assessment)
2022 Rapid prenatal testing for common aneuploidies GenQA (Genomics Quality Assessment)
2023 Rapid prenatal testing for common aneuploidies GenQA (Genomics Quality Assessment)
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