Uniparental DisomyPrader-Willi SyndromeChromosomes, Human, Pair 15Genomic ImprintingAngelman SyndromeBeckwith-Wiedemann SyndromeChromosome MappingMosaicismChromosome AberrationsChromosomesChromosomes, Human, Pair 7Chromosomes, Human, Pair 14Chromosomes, Human, Pair 11KaryotypingAneuploidyMacroglossiaNondisjunction, GeneticTrisomyChromosome BandingFathersChromosome DeletionChromosomes, Human, Pair 6Chromosomes, Human, Pair 1Chromosomes, HumanChromosomes, Human, Pair 13Chromosome DisordersIn Situ Hybridization, FluorescenceX ChromosomeAbnormalities, MultipleChorionic Villi SamplingsnRNP Core ProteinsSilver-Russell SyndromeChromosomes, Human, Pair 20Chromosomes, Human, YMicrosatellite RepeatsSex ChromosomesLoss of HeterozygosityPedigreeIsochromosomesChromosomes, Human, Pair 21Genetic MarkersTranslocation, GeneticChromosomes, Human, Pair 17Chromosome InversionGrowth DisordersSteatorrheaChromosome SegregationMyelodysplastic-Myeloproliferative DiseasesSyndromePhenotypeChromosomes, BacterialHernia, UmbilicalMothersPolymorphism, Single NucleotideChromosomes, Human, Pair 9HomozygoteDwarfismRNA, Long NoncodingChromosomes, FungalChromosomes, Human, Pair 16Chromosomes, Human, Pair 18AllelesChromosomes, PlantDNA MethylationMutationChromosomes, Human, 6-12 and XChromosomes, Human, Pair 4Chromosomes, Human, Pair 8Chromosomes, Human, Pair 2Chromosomes, Human, Pair 22Chromosome PairingChromosomes, MammalianBase SequenceChromosomes, Human, Pair 10Cytogenetic AnalysisGene DosageChromosomes, Human, Pair 19BivalviaBlotting, SouthernFetal Growth RetardationChromosomes, Artificial, BacterialChromosomes, Human, XChromosomes, Human, 1-3Chromosomes, Human, Pair 12Chromosome PaintingChromosomes, Human, Pair 5Genome, HumanGenotypeDNA Mutational AnalysisChromosomes, Human, 16-18HeterozygoteMyeloproliferative DisordersChromosomes, Artificial, YeastProto-Oncogene Proteins c-cblOligonucleotide Array Sequence AnalysisChromosomes, Human, 13-15MeiosisRibonucleoproteins, Small NuclearGenetic LinkageMolecular Sequence Data