Muscular DystrophiesMuscular Dystrophy, DuchenneSex RatioMuscular Dystrophy, AnimalMaltaDystrophinBirth RateMice, Inbred mdxMuscular Dystrophies, Limb-GirdleMyotonic DystrophyMuscular Dystrophy, FacioscapulohumeralKlinefelter SyndromeMuscular Dystrophy, Emery-DreifussUtrophinSarcoglycansDystroglycansInfant, NewbornCorneal Dystrophies, HereditaryMuscle, SkeletalMuscular Dystrophy, OculopharyngealPregnancyBirth WeightHeterozygote DetectionFuchs' Endothelial DystrophyDystrophin-Associated ProteinsSarcolemmaPedigreeThymopoietinsCreatine KinaseMuscle Fibers, SkeletalRetinal DystrophiesCollagen Type VIMusclesExonsMyoblastsX ChromosomeMuscle ProteinsPremature BirthDystrophin-Associated Protein ComplexNeuromuscular DiseasesCaveolin 3MutationLamininMuscular DiseasesDisease Models, AnimalPhenotypeChromosomes, Human, Pair 4Lamin Type ACytoskeletal ProteinsInfant, Low Birth WeightCardiomyopathiesGenetic LinkagePoly(A)-Binding Protein IIGenetic TherapyDiaphragmRegenerationMuscle StrengthNeuroaxonal DystrophiesMuscle DevelopmentHeterozygoteGenes, RecessiveMice, Inbred C57BLSarcoglycanopathiesWalker-Warburg SyndromeCalpainPregnenedionesMuscle WeaknessPrenatal DiagnosisMembrane ProteinsMolecular Sequence DataMyostatinPlectinSatellite Cells, Skeletal MuscleDependovirusMorpholinosDNA Mutational AnalysisMyositisBirth OrderConsanguinityGenetic CounselingChromosome MappingBirth CertificatesConnectinImmunohistochemistryReflex Sympathetic DystrophyBase SequenceSyndromeCardiomyopathy, DilatedMyoblasts, SkeletalPolymerase Chain ReactionMice, TransgenicMuscle CellsBiopsyVitelliform Macular DystrophyChromosome DeletionElectroretinographyGenetic TestingGene DeletionMice, KnockoutGenes, Dominant