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Market Research Report
Product code
974400
Inborn Gene or Chromosome Alterations Tests - Medical Devices Pipeline Assessment, 2020 |
Inborn Gene or Chromosome Alterations Tests - Medical Devices Pipeline Assessment, 2020 |
Published: November 30, 2020
GlobalData
Content info: 314 Pages
Delivery time: 1-2 business days
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GlobalData's Medical Devices sector report, "Inborn Gene or Chromosome Alterations Tests - Medical Devices Pipeline Assessment, 2020" provides comprehensive information about the Inborn Gene or Chromosome Alterations Tests pipeline products with comparative analysis of the products at various stages of development and information about the clinical trials which are in progress.
Inborn Gene or Chromosome Alterations Tests are the genetic tests used to detect monogenetic disorders (like Cystic Fibrosis, Haemochromatosis, Prothrombin Mutation etc), polygenetic disorders (like Asthma , Atherosclerosis, Diabetes, Hypertension, Osteoporosis, etc), chromosomal disorders (like Down's Syndrome, Edwards Syndrome etc), polymorphisms (like HLA-Typing etc).
Note: Certain sections in the report may be removed or altered based on the availability and relevance of data in relation to the equipment type.
The report enables you to -