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The basis of this syndrome remains to be determined; autoimmune disease, chromosomal breakage syndromes, and other neurocutaneous syndromes have been excluded.<\/jats:p>","DOI":"10.1136\/jmg.29.8.592","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:23:16Z","timestamp":1226330596000},"page":"592-594","source":"Crossref","is-referenced-by-count":3,"title":["Progressive vitiligo, mental retardation, facial dysmorphism, and urethral duplication without chromosomal breakage or immunodeficiency."],"prefix":"10.1136","volume":"29","author":[{"given":"P","family":"Labrune","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R","family":"Assathiany","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D","family":"Penso","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M","family":"Odi\u00e8vre","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1992,8,1]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"945","DOI":"10.1002\/ajmg.1320300412","article-title":"The Ermine phenotype: pigmentary-hearing loss heterogeneity","volume":"30","author":"O'Doherty, N.J.; Gorlin, R.J.","year":"1988","unstructured":"O'Doherty NJ, Gorlin RJ. 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