Current status of prenatal diagnosis by DNA analysis

Keyphrases

• Prenatal Diagnosis 100%
• DNA Analysis 100%
• Hemophilia 100%
• Direct Detection 83%
• β-Thalassemia (β-thal) 50%
• Cystic Fibrosis 33%
• Sickle Cell Anemia 33%
• Duchenne muscular Dystrophy 33%
• Indirect Detection 33%
• Gene Diagnosis 33%
• Working Hard 16%
• Disease Genes 16%
• Polycystic Kidney Disease 16%
• Huntington's Disease 16%
• X-linked Disorder 16%
• Alpha-1 Antitrypsin Deficiency 16%
• Neurofibromatosis 16%
• Novel Technique 16%
• Becker muscular Dystrophy 16%
• Finite number 16%
• Hemophilia B 16%
• α-thalassemia 16%
• Detection Mode 16%

Medicine and Dentistry

• DNA Determination 100%
• Haemophilia A 100%
• Prenatal Diagnosis 100%
• Beta Thalassemia 60%
• Cystic Fibrosis 40%
• Sickle-Cell Disease 40%
• Duchenne Muscular Dystrophy 40%
• Allele 20%
• Polycystic Kidney Disease 20%
• X Chromosome Linked Disorder 20%
• Neurofibromatosis 20%
• Huntington's Disease 20%
• Becker Muscular Dystrophy 20%
• Haemophilia B 20%
• Alpha 1-Antitrypsin Deficiency 20%
• Alpha-Thalassemia 20%

Pharmacology, Toxicology and Pharmaceutical Science

• Haemophilia A 100%
• Beta Thalassemia 60%
• Cystic Fibrosis 40%
• Sickle Cell Anemia 40%
• Duchenne Muscular Dystrophy 40%
• X Chromosome Linked Disorder 20%
• Huntington Chorea 20%
• Kidney Polycystic Disease 20%
• Becker Muscular Dystrophy 20%
• Neurofibromatosis 20%
• Haemophilia B 20%
• Alpha Thalassemia 20%
• Alpha 1 Antitrypsin Deficiency 20%