Growth DisordersDwarfismBody HeightTurner SyndromeAge Determination by SkeletonOsteochondrodysplasiasDwarfism, PituitaryAbnormalities, MultipleNoonan SyndromeBone Diseases, DevelopmentalSyndromeHuman Growth HormoneMicrocephalyAchondroplasiaPuberty, DelayedIntellectual DisabilityGonadal Dysgenesis, MixedGrowth HormonePubertyMetacarpusPedigreeHand Deformities, CongenitalHypertrichosisLaron SyndromeCephalopelvic DisproportionConsanguinityGrowth ChartsPuberty, PrecociousDysostosesPhenotypeFailure to ThriveFaceFacial BonesOsteopoikilosisSex Chromosome AberrationsCleidocranial DysplasiaPelger-Huet AnomalyGenes, RecessiveMutationMental Retardation, X-LinkedLipoid Proteinosis of Urbach and WietheKaryotypingInsulin-Like Growth Factor IChromosome DisordersAnthropometryLimb Deformities, CongenitalBone DevelopmentGrowthInfant, NewbornPseudohypoparathyroidismChromosomes, Human, XPigmentation DisordersArm BonesCraniofacial AbnormalitiesFaciesHomeodomain ProteinsBrachydactylyOptic AtrophyHaploinsufficiencyChromosome DeletionHypopituitarismSchizoid Personality DisorderBone LengtheningMusculoskeletal AbnormalitiesOsteogenesis, DistractionReceptors, SomatotropinChild Nutrition DisordersBone and BonesMosaicismMutation, MissenseDNA Mutational AnalysisEndocrine System DiseasesRing ChromosomesBody WeightMicrognathismIlizarov TechniqueX ChromosomeCodon, NonsenseHomozygoteChondrodysplasia PunctataChromosome MappingHormone Replacement TherapyNephrocalcinosisHypogonadismHeterozygoteEllis-Van Creveld SyndromeRothmund-Thomson SyndromeGenu ValgumChild DevelopmentSodium BenzoateSkin AbnormalitiesMouth AbnormalitiesDevelopmental DisabilitiesReference ValuesOxymetholoneChromosomes, Human, Pair 12Prader-Willi SyndromeGenes, DominantRubinstein-Taybi SyndromeInsulin-Like Growth Factor Binding Protein 3