Genetic Diseases, InbornProtoporphyria, ErythropoieticMetabolism, Inborn ErrorsPedigreeMutationBipolar DisorderGranulomatous Disease, ChronicSyndromeFerrochelataseMental DisordersPorphyria, HepatoerythropoieticAnxiety DisordersMood DisordersGenes, RecessiveJaundice, Chronic IdiopathicAmino Acid Metabolism, Inborn ErrorsLipid Metabolism, Inborn ErrorsHepatolenticular DegenerationPhenotypeHemochromatosisIchthyosisDNA Mutational AnalysisHypophosphatasiaHemoglobinopathiesDiagnostic and Statistical Manual of Mental DisordersHeterozygoteGitelman SyndromeGenes, DominantIchthyosiform Erythroderma, CongenitalMolecular Sequence DataGenetic LinkageMutation, MissenseHomozygotePurine-Pyrimidine Metabolism, Inborn ErrorsMyasthenic Syndromes, CongenitalPhotosensitivity DisordersPrenatal DiagnosisGenetic TestingDepressive Disorder, MajorTooth AbnormalitiesBase SequenceFrameshift MutationChromosome MappingAttention Deficit Disorder with HyperactivityCodon, NonsenseRefsum DiseaseDisease Models, AnimalAcyl-CoA DehydrogenaseFamilial Mediterranean FeverGenotypeDepressive DisorderGenetic Predisposition to DiseaseExonsAdrenoleukodystrophyObsessive-Compulsive DisorderStress Disorders, Post-TraumaticAutistic DisorderHeterozygote DetectionPoint MutationAbnormalities, MultiplePhobic DisordersChild Development Disorders, PervasivePsychotic DisordersSubstance-Related DisordersMalignant HyperthermiaAllelesLong QT SyndromeGenetic TherapyAge of OnsetAmino Acid SequenceIntellectual DisabilityPolymerase Chain ReactionFibroblastsFamily HealthConduct DisorderInfant, NewbornX ChromosomeCells, CulturedLod ScoreMembrane ProteinsTic DisordersDNAGenetic MarkersPsychiatric Status Rating ScalesGerm-Line MutationSkinBorderline Personality DisorderNADPH OxidasePolymorphism, GeneticPolymorphism, Single-Stranded ConformationalHaplotypesSomatoform DisordersCation Transport ProteinsSequence DeletionCognition DisordersSleep DisordersGenetic VectorsLiverIronGene Transfer Techniques