Vitamin A DeficiencyDeficiency Diseasesalpha 1-Antitrypsin DeficiencyVitamin B 12 DeficiencyVitamin D DeficiencyFolic Acid DeficiencyIgA DeficiencyThiamine DeficiencyGlucosephosphate Dehydrogenase DeficiencyMagnesium DeficiencyAnemia, Iron-DeficiencyVitamin E DeficiencyAscorbic Acid DeficiencyMice, KnockoutImmunologic Deficiency SyndromesProtein C DeficiencyIgG DeficiencyVitamin B 6 DeficiencyFactor V DeficiencyIronRiboflavin DeficiencyMutationAntithrombin III DeficiencyMice, Inbred C57BLMetabolism, Inborn ErrorsVitamin K DeficiencyFactor VII DeficiencyFactor XI DeficiencyProtein DeficiencyAnemia, HypochromicVitamin B DeficiencyFactor XIII DeficiencyLeukocyte-Adhesion Deficiency SyndromeIodineZincPhenotypeFactor X DeficiencyOrnithine Carbamoyltransferase Deficiency DiseaseAdrenal Hyperplasia, CongenitalHomozygoteCholine DeficiencyLiverCytochrome-c Oxidase DeficiencyAmino Acid Metabolism, Inborn ErrorsHeterozygotePedigreeDisease Models, AnimalLecithin Acyltransferase DeficiencyBiotinidase DeficiencyVitamin B 12FerritinsDietYin DeficiencyMolecular Sequence DataBase SequenceLipid Metabolism, Inborn ErrorsVitamin Dalpha 1-AntitrypsinMice, Mutant StrainsHypopituitarismCarbohydrate Metabolism, Inborn ErrorsFatty Acids, EssentialPurine-Pyrimidine Metabolism, Inborn ErrorsSteroid 21-HydroxylaseCells, CulturedVitamin AHuman Growth HormoneMice, TransgenicFibroblastsHemoglobinsIron, DietaryDwarfism, PituitaryRNA, MessengerCopperErythrocytesInfant, NewbornAnemia, HemolyticPotassium DeficiencyPlatelet Storage Pool DeficiencyFolic AcidDietary SupplementsBody WeightSeleniumConsanguinityPregnancyGrowth DisordersMethylmalonic AcidGenotypeErythrocyte IndicesPoint MutationCarnitineDihydropyrimidine Dehydrogenase DeficiencyMutation, MissenseBrain Diseases, Metabolic, InbornNutritional StatusAcyl-CoA DehydrogenasesPyruvate Dehydrogenase Complex Deficiency DiseaseAllelesGlucosephosphate DehydrogenaseGene Deletion