Mikrogen - Experting Reproductive Genetics
Experting Reproductive Genetics
Mikrogen
About Us
Why Mikrogen?
Mission-Vision
Quality Policy
Gallery
Our Team
Business Partners
Career
PDPA
Accreditation
Medical Tourism
References
Genetic Counseling
Test Guide
Test Requisition Forms
Test Catalog
Whole Exome / Genome Sequencing
Immunology
Prenatal Genetic Tests
Cardiology
Malformation and Retardation Syndromes
Endocrine Diseases
Skeletal, Connective Tissue and Skin Diseases
Andrology
Obstetrics / Infertility
Metabolic Diseases
Oncogenetics / Pharmacogenetics
Hematology – Oncology
Cytogenetics
Neurology / Muscle Diseases
Other
PGT
PGT-A
PGT-M
PGT-SR
Combined PGT
Scientific Studies
Projects
Project Partners
Publications
Contacts
Corporate & Portal Login
CORPORATE LOGIN
LIOS
ALIS
PORTAL LOGIN
Toggle menu
Search Test
Other
Mikrogen
>
Genetic Tests
>
Other
Other
Eye Diseases Panel (349 Genes)
Other
Nephrology Panel (68 Genes)
Other
CarrierCheck Carrier Test (462 genes) (Solo)
Other
CarrierCheck Carrier Test (462 genes) (Duo)
Other
CarrierCheck Carrier Test (146 genes) (Duo)
Other
CarrierCheck Carrier Screening Test (146 genes) (Solo)
Other
GDF1 Whole Gene Sequencing Test
Other
H3F3B Gene K36M Mutation Screening Test
Other
Single Region Sequence Analysis (6 Mutations)
Other
Single Region Sequence Analysis (5 Mutations)
Other
Single Region Sequence Analysis (4 Mutations)
Other
LMNA Deletion Duplication Analysis
Other
TWNK Whole Gene Sequencing
Other
Crohn Inflammatory Bowel Disease (84 Genes)
Other
Tubular Nephrotic Syndrome Panel (42 Genes)
Other
Treacher Collins Syndrome Panel (3 Genes)
Other
Congenital Glaucoma Panel (6 Genes)
Other
Isolated GNHR Deficiency Panel (8 Genes)
Other
Molecular Karyotyping (Whole Genome Deletion duplication)
Other
DNA Fingerprinting
Other
Whole Genome Sequencing -Trio
Other
Whole Genome Sequencing -Duo
Other
Whole Genome Sequencing – Solo
Other
Whole Exome Sequencing – Trio
Other
Whole Exome Sequencing – Duo
Other
Whole Exome Sequencing – Solo
Other
Factor VII Deficiency
Other
Progressive Erythrokeratoderma
Other
Hyperphenylalaninemia
Other
Hereditary Xanthinuria Type 2
Other
5-Oxoprolinase Deficiency
Other
Hyperlipoproteinemia Type 1B
Other
WARS2 Sequence Analysis
Other
Peters-plus syndrome
Other
Urbach-Wiethe Disease
Other
SCN1A MLPA
Other
Frank-ter Haar Syndrome
Other
Trichohepatoenteric Syndrome Type 2
Other
Cobalamin Metabolism Disorder
Other
Multiple Epiphyseal Dysplasia Type 5
1
2
3
4
Next page