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Genet."],"published-print":{"date-parts":[[1989,5]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>We report a 6\u2010month\u2010old boy, born of consanguineous (first\u2010cousin) parents (F = 1\/16) presenting microbrachycephaly, wide forehead, marked hypertelorism, broad nose with a midline groove with a bilateral small \u201cblind dimple\u201d in each side, hypospadias, syndactyly between fingers 3 and 4, broad thumbs, and halluces. This association of anomalies suggests the diagnosis of a \u201cnew\u201d type of acrofronto\u2010facio\u2010nasal dysostosis. Normal chromosomes, parental consanguinity, and familial occurrence suggest autosomal recessive inheritance.<\/jats:p>","DOI":"10.1002\/ajmg.1320330118","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T02:59:47Z","timestamp":1118545187000},"page":"121-124","source":"Crossref","is-referenced-by-count":20,"title":["Autosomal recessive acro\u2010fronto\u2010facio\u2010nasal dysostosis associated with genitourinary anomalies"],"prefix":"10.1002","volume":"33","author":[{"given":"A.","family":"Richieri\u2010Costa","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Montagnoli","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"T. 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