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In addition to the characteristic facial and limb defects, previously undescribed anomalies, including midgut malrotation, gastric volvulus, and renal anomalies, are recorded.<\/jats:p>","DOI":"10.1136\/jmg.28.10.695","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:11:11Z","timestamp":1226329871000},"page":"695-700","source":"Crossref","is-referenced-by-count":25,"title":["Miller syndrome (postaxial acrofacial dysostosis): further evidence for autosomal recessive inheritance and expansion of the phenotype."],"prefix":"10.1136","volume":"28","author":[{"given":"A L","family":"Ogilvy-Stuart","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A C","family":"Parsons","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1991,10,1]]},"reference":[{"key":"ref_1","first-page":"87","article-title":"Recurrence of the postaxial acrofacial dysostosis syndrome: implications for genetic counseling","volume":"98","author":"Fineman, R.M.","year":"1981","unstructured":"Fineman RM. 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