MicrocephalyAbnormalities, MultipleIntellectual DisabilitySyndromeConsanguinityFaciesGenes, RecessiveLissencephalyNijmegen Breakage SyndromeMicrognathismDwarfismInfant, NewbornPedigreeDevelopmental DisabilitiesPhenylketonuria, MaternalGrowth DisordersAgenesis of Corpus CallosumCentrosomeOptic AtrophyNerve Tissue ProteinsKaryotypingSegmental Duplications, GenomicChromosome DisordersPhenotypeCri-du-Chat SyndromeExomeMandibulofacial DysostosisHeadChromosome BreakageCentriolesCraniofacial Abnormalities