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Polygenic Risk Score - Coronary artery diseases
Polygenic Risk Score - Breast Cancer
NIPT Monogenic
Liquid Biopsy
Optical Genome Mapping (OGM)
RNA-Sequencing
Repeat-Panel-Anaylses
FSHD testing
Epigenetic Signature
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Gene Panel Sequencing
Single Gene Analysis
Exome Sequencing
Repeat-Expansion Analysis
Methylation Analysis
Deletion/Duplication Analysis
Carrier Screening
Prenatal NGS analyses
Cytogenetics And Microarray Analysis
About Genetic Counseling
About Genetic Testing
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Beyond Exome
Polygenic Risk Score - Coronary artery diseases
Polygenic Risk Score - Breast Cancer
NIPT Monogenic
Liquid Biopsy
Optical Genome Mapping (OGM)
RNA-Sequencing
Repeat-Panel-Anaylses
FSHD testing
Epigenetic Signature
Test Catalog
How to order
How to Order a Genetic Test
Cost & Billing Information
Sample Requirements
Shipping Instructions
Genetic Testing
Gene Panel Sequencing
Single Gene Analysis
Exome Sequencing
Repeat-Expansion Analysis
Methylation Analysis
Deletion/Duplication Analysis
Carrier Screening
Prenatal NGS analyses
Cytogenetics And Microarray Analysis
Patients & Clinicians
About Genetic Counseling
About Genetic Testing
Downloads
FAQ
About MGZ
What We Do
Why MGZ?
The MGZ Team
Quality Management
Test Catalog
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Muscle Diseases
Glycogen storage disease type II - GAA
includes 1 Gene(s)
McArdle Disease I PYGM
includes 1 Gene(s)
Congenital myasthenic syndrome (CMS)
includes 36 Gene(s)
Muscle weakness (myopathy, muscular dystrophy) - comprehensive panel
includes 244 Gene(s)
CPEO (Chronic progressive external ophthalmoplegia), nuclear
includes 12 Gene(s)
Muscular dystrophy, Duchenne / Becker (Dystrophinopathy)
includes 1 Gene(s)
Muscular dystrophy, congenital, dystroglycanopathy
includes 15 Gene(s)
Muscular dystrophy, type Emery-Dreifuss
includes 4 Gene(s)
Muscle weakness, early-onset, Floppy Infant
includes 136 Gene(s)
FSHD2
includes 3 Gene(s)
Muscular dystrophy, limb-girdle - core panel
includes 9 Gene(s)
Muscular dystrophy, congenital, collagen-associated (Bethlem/Ullrich and phenocopies)
includes 7 Gene(s)
Muscular dystrophy, congenital, entire panel
includes 29 Gene(s)
CK-elevation, isolated
includes 11 Gene(s)
Myopathy, mitochondrial, nuclear genes
includes 20 Gene(s)
Myalgia, muscle cramps
includes 11 Gene(s)
Muscle weakness, adult-onset
includes 108 Gene(s)
Myopathy, myofibrillar
includes 9 Gene(s)
Myopathy, distal / Inclusion body myopathy
includes 9 Gene(s)
Muscle disease with contractures and/or rigid spine
includes 26 Gene(s)
Myopathy, congenital - nemaline / core / centronuclear
includes 19 Gene(s)
Myopathy, congenital - centronuclear
includes 5 Gene(s)
Metabolic myopathy and rhabdomyolysis
includes 33 Gene(s)
CPEO (Chronic progressive external ophthalmoplegia), nuclear genes and phenocopies
includes 35 Gene(s)
Apneas, neonatal
includes 13 Gene(s)
Muscular dystrophy, scapuloperoneal syndrome
includes 9 Gene(s)