• Home
  • Disorders
  • GeneReviews
  • Genes
  • Panels
  • Laboratories
  • Clinics
    • Select One: Disorders Genes Panels

Products found: 347Search results

Dr. Eberhard and Partner, MVZ Dortmund

Disorder Genes Test Method Lab Info Product code  
Dr. Eberhard and Partner, MVZ Dortmund 11-beta-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP11B1, Sequence analysis of the entire coding region
Dr. Eberhard and Partner, MVZ Dortmund 17-alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP17A1, Sequence analysis of the entire coding region
Dr. Eberhard and Partner, MVZ Dortmund 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP21A2, Deletion/duplication analysis
Dr. Eberhard and Partner, MVZ Dortmund 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia CYP21A2, Sequence analysis of the entire coding region
Dr. Eberhard and Partner, MVZ Dortmund 3-beta-Hydroxysteroid Dehydrogenase-Deficient Congenital Adrenal Hyperplasia HSD3B2, Sequence analysis of the entire coding region
Dr. Eberhard and Partner, MVZ Dortmund Acrodermatitis Enteropathica, Zinc-Deficiency Type SLC39A4, Sequence analysis of the entire coding region
Dr. Eberhard and Partner, MVZ Dortmund Acute Intermittent Porphyria HMBS, Sequence analysis of the entire coding region
Dr. Eberhard and Partner, MVZ Dortmund ACVRL1-Related Hereditary Hemorrhagic Telangiectasia ACVRL1, Sequence analysis of the entire coding region
Dr. Eberhard and Partner, MVZ Dortmund Alpha-Thalassemia HBA1, HBA2, HBZ, Deletion/duplication analysis
Dr. Eberhard and Partner, MVZ Dortmund Alpha-Thalassemia HBA1, HBA2, HBZ, Sequence analysis of the entire coding region
Dr. Eberhard and Partner, MVZ Dortmund Alpha-Thalassemia HBA1, HBA2, HBZ, Targeted mutation analysis
Dr. Eberhard and Partner, MVZ Dortmund Alpha-Thalassemia X-Linked Intellectual Disability Syndrome ATRX, Deletion/duplication analysis
Loading...