[On the heterozygote carrier of congenital metabolic diseases. 2].
D005826:Genetics, Medical; D006008:Glycogen Storage Disease; D006527:Hepatolenticular Degeneration; D006579:Heterozygote; D006801:Humans; D006932:Hyperbilirubinemia; D008659:Metabolic Diseases; D009136:Muscular Dystrophies
GENETICS, HUMAN; GLYCOGENOSIS; HEPATOLENTICULAR DEGENERATION; HYPERBILIRUBINEMIA; METABOLIC DISEASES; MUSCULAR DYSTROPHY