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The latter case represents overlap of the Hallermann\u2013Streiff syndrome and oculodentodigital dysplasia. \u201cDwarfism\u201d as a possible clinical risk marker of mental retardation is discussed. As cause, a mendelian autosomal dominant mutation seems most probable.<\/jats:p>","DOI":"10.1002\/ajmg.1320410428","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T04:31:54Z","timestamp":1118550714000},"page":"517-520","source":"Crossref","is-referenced-by-count":16,"title":["Hallermann\u2013Streiff syndrome: Clinical and psychological findings in children. Nosologic overlap with oculodentodigital dysplasia?"],"prefix":"10.1002","volume":"41","author":[{"given":"Ann","family":"Spaepen","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Constance","family":"Schrander\u2010Stumpel","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jean\u2010Pierre","family":"Fryns","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christine","family":"De Die\u2010Smulders","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Martine","family":"Borghgraef","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Herman","family":"Van Den Berghe","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2005,6,3]]},"reference":[{"key":"e_1_2_1_2_1","first-page":"261","article-title":"Syndrome de Fran\u00e7ois. 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