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The finding of an extra bone within the anterior fontanel in our patient suggests similarity to the Xt mouse mutant, which is homologous to Greig syndrome in man. This provides additional support for the hypothesis of allelism of the Greig and acrocallosal syndromes.<\/jats:p>","DOI":"10.1002\/ajmg.1320350325","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T23:45:23Z","timestamp":1118533523000},"page":"443-446","source":"Crossref","is-referenced-by-count":24,"title":["Acrocallosal syndrome"],"prefix":"10.1002","volume":"35","author":[{"given":"Han J. E.","family":"Hendriks","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Han G.","family":"Brunner","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ton A. M.","family":"Haagen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ben C. 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