Ozcelik, T.2018-04-122018-04-1220081559-0267http://hdl.handle.net/11693/38115[No abstract available]EnglishAutoimmune diseasesFemale predispositionMosaicismX chromosome inactivationAndrogen receptorMelanoma antigenChromosome translocationClinical featureDisease associationDisease courseDisease predispositionDuchenne muscular dystrophyFragile X syndromeGene expressionGene locusGene mutationGenetic linkageGenetic traitGenetic variabilityHematopoietic stem cellHeterozygosityHumanImmunological toleranceReviewSclerodermaWiskott Aldrich syndromeX chromosome inactivationX chromosome linked disorderX linked agammaglobulinemiaX linked mental retardationAutoimmunityFemaleGenetic Predisposition to DiseaseHumansMaleMutationScleroderma, SystemicSex CharacteristicsX Chromosome InactivationX chromosome inactivation and female predisposition to autoimmunityArticle10.1007/s12016-007-8051-0