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Syndromes of ulnar ray reduction are briefly reviewed and the relationship between limb bud and midline development discussed.<\/jats:p>","DOI":"10.1136\/jmg.29.9.659","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:23:16Z","timestamp":1226330596000},"page":"659-662","source":"Crossref","is-referenced-by-count":17,"title":["Weyers' ulnar ray\/oligodactyly syndrome and the association of midline malformations with ulnar ray defects."],"prefix":"10.1136","volume":"29","author":[{"given":"P D","family":"Turnpenny","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J C","family":"Dean","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P","family":"Duffty","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J A","family":"Reid","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P","family":"Carter","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","published-online":{"date-parts":[[1992,9,1]]},"reference":[{"key":"ref_1","first-page":"961","article-title":"Congenital malformations","author":"Warkany, J.","year":"1971","unstructured":"Warkany J. Congenital malformations. Chicago: Yearbook Medical Publishers, 1971:961-2."},{"key":"ref_2","first-page":"351","article-title":"Das oligodactylie-syndrom des menschen und seine parallelmutation bei der hausmaus","volume":"189","author":"Weyers, H.","year":"1957","unstructured":"Weyers H. Das oligodactylie-syndrom des menschen und seine parallelmutation bei der hausmaus. Ann Paediatr 1957;189:351-70."},{"key":"ref_3","doi-asserted-by":"crossref","first-page":"170","DOI":"10.1111\/j.1399-0004.1987.tb02790.x","article-title":"Roberts syndrome and SC phocomelia. A single genetic entity","volume":"31","author":"Romke, C.; Froster-Iskenius, U.; Heyne, K.","year":"1987","unstructured":"Romke C, Froster-Iskenius U, Heyne K, et al. Roberts syndrome and SC phocomelia. A single genetic entity. 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