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dc.contributor.authorJ Gordon Millichap
dc.contributor.otherNorthwestern University Feinberg School of Medicine
dc.date.accessioned2016-09-29T14:35:26Z
dc.date.available2025-10-02T03:51:25Z
dc.date.issued01-09-1999
dc.identifier.issn-
dc.identifier.urihttps://www.pediatricneurologybriefs.com/articles/1990
dc.description.abstractEvidence purporting that the so-called hypomelanosis of Ito (HI) syndrome does not exist as a distinct multisystem birth defect is presented by geneticists and dermatologists at Bad Salzschlirf, and Philipp University of Marburg, Germany.
dc.format-
dc.language.isoEN
dc.publisherPediatric Neurology Briefs Publishers
dc.relation.uri['https://maat.journals.ekb.eg/journal/aim_scope', 'https://maat.journals.ekb.eg/journal/authors.note', 'https://maat.journals.ekb.eg/']
dc.rightsCC BY-NC
dc.subject['music', 'art', 'education', 'teaching', 'information technology', 'Special aspects of education', 'LC8-6691', 'Music', 'M1-5000', 'Fine Arts', 'N']
dc.subject.lccPediatrics
dc.titleHypomelanosis of Ito: A Genetic Mosaicism
dc.typeArticle
dc.description.keywordshypomelanosis of ito
dc.description.keywordsincontinentia pigmenti achromians
dc.description.keywordspigmentary dysplasia
dc.description.pages67-67
dc.description.doi10.15844/pedneurbriefs-13-9-4
dc.title.journalPediatric Neurology Briefs
dc.identifier.e-issn2166-6482
dc.identifier.oaioai:doaj.org/journal:635b3b27f12d4660b0215790aa378551
dc.journal.infoVolume 13, Issue 9


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