EMEDICINE RESULTS
95 documents matched mitochondrial DNA in population genetics
Industry Information
- Ataxia with Identified Genetic and Biochemical Defects (Neurology)
- MELAS Syndrome (Pediatrics: Genetics and Metabolic Disease)
- Genetic and Inflammatory Mechanisms in Stroke (Neurology)
- Kearns-Sayre Syndrome (Pediatrics: Genetics and Metabolic Disease)
- Oculocerebrorenal Dystrophy (Lowe Syndrome) (Pediatrics: Genetics and Metabolic Disease)
- Inner Ear, Genetic Sensorineural Hearing Loss (Otolaryngology and Facial Plastic Surgery)
- Arthrogryposis (Pediatrics: Genetics and Metabolic Disease)
- Hyperammonemia-Hyperornithinemia-Homocitrullinemia Syndrome (Pediatrics: Genetics and Metabolic Disease)
- Tetrahydrobiopterin Deficiency (Pediatrics: Genetics and Metabolic Disease)
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency (Pediatrics: Genetics and Metabolic Disease)
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