Campomelic DysplasiaSOX9 Transcription FactorBone Diseases, DevelopmentalOsteochondrodysplasiasHigh Mobility Group ProteinsAbnormalities, MultipleDisorders of Sex DevelopmentSyndromeGonadal Dysgenesis, 46,XYSmith-Lemli-Opitz SyndromeChromosomes, Human, Pair 17Musculoskeletal AbnormalitiesTeratogensAbnormalities, Drug-InducedBone and BonesSteroid Metabolism, Inborn ErrorsMouth AbnormalitiesFetal ResorptionChondrodysplasia PunctataUrogenital AbnormalitiesEctromeliaTranscription FactorsArteriovenous MalformationsCraniofacial AbnormalitiesTranslocation, GeneticInfant, NewbornOxidoreductases Acting on CH-CH Group DonorsPhenotypeMutationMolecular Sequence DataPregnancyFibrous Dysplasia of BoneArnold-Chiari MalformationPedigreeEctodermal DysplasiaVascular MalformationsBronchopulmonary Dysplasia