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pubmed-article:15327534pubmed:abstractTextThere is increasing evidence that hypomelanosis of Ito and related disorders such as linear and whorled naevoid hypermelanosis are due to mosaicism for a variety of chromosomal abnormalities. This group of disorders is better termed 'pigmentary mosaicism'. In this review we explain how disparate chromosomal abnormalities might manifest as a common pigmentary phenotype. In particular, we provide evidence supporting the hypothesis that the chromosomal abnormalities reported in these disorders specifically disrupt expression or function of pigmentary genes.lld:pubmed
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pubmed-article:15327534pubmed:year2004lld:pubmed
pubmed-article:15327534pubmed:articleTitleAbnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes.lld:pubmed
pubmed-article:15327534pubmed:affiliationDepartment of Dermatology, Birmingham Children's Hospital, Birmingham, UK. s.taibjee@virgin.netlld:pubmed
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