PedigreeGenes, DominantGenetic Diseases, InbornInheritance PatternsGenetic LinkageGenetic CounselingChromosome MappingMutationGenetic TestingLod ScoreGenes, RecessivePhenotypeHeterozygoteHand Deformities, CongenitalFamily HealthSyndromeDystonia Musculorum DeformansWilliams SyndromeChromosome DisordersAbnormalities, MultipleFoot Deformities, CongenitalGenetic Predisposition to DiseaseUltimobranchial BodyHypertelorismSyndactylyPenetranceChromosomesDNA Mutational AnalysisGenetic MarkersToesAge of OnsetChromosomes, Human, Pair 16Chromosome AberrationsHaplotypesGenetic HeterogeneityGenotypeMicrosatellite RepeatsMutation, MissenseX ChromosomePolycystic Kidney, Autosomal DominantMolecular Sequence DataCrosses, GeneticBase SequenceAllelesModels, GeneticChromosome BandingFamilyRetinitis PigmentosaChromosomes, Human, Pair 1Chromosomes, Human, Pair 12Polymerase Chain ReactionSex ChromosomesConsanguinityChromosomes, Human, Pair 7Chromosomes, HumanChromosomes, Human, Pair 17Chromosomes, Human, Pair 11Chromosome SegregationChromosomes, Human, Pair 6Myotonia CongenitaChromosomes, Human, Pair 2Chromosomes, BacterialChromosomes, Human, Pair 9Muscle CrampPoint MutationPolymorphism, GeneticChromosomes, Human, Pair 19Chromosome DeletionSequence Analysis, DNAChromosomes, Human, Pair 4Chromosomes, PlantChromosomes, Human, Pair 21Chromosomes, Human, Pair 10Chromosomes, Human, Pair 13Chromosomes, FungalChromosomes, Human, Pair 5Chromosomes, Human, Pair 22DNAChromosomes, Human, 6-12 and XChromosomes, Human, Pair 8HomozygoteExonsChromosomes, MammalianChromosomes, Human, Pair 15Cleft LipChromosomes, Human, 1-3Chromosome PairingChromosomes, Human, Pair 20DNA, MitochondrialChromosomes, Human, YChromosomes, Human, XChromosomes, Human, Pair 14Genetic VariationChromosomes, Human, Pair 18TRPP Cation ChannelsChromosomes, Artificial, BacterialKaryotypingIn Situ Hybridization, FluorescenceChromosome PaintingChromosomes, Artificial, Yeast