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However, chromosome analysis has not detected any structural abnormality in our patients.<\/jats:p>","DOI":"10.1136\/jmg.28.6.389","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:11:11Z","timestamp":1226329871000},"page":"389-394","source":"Crossref","is-referenced-by-count":34,"title":["Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal\/duodenal atresia."],"prefix":"10.1136","volume":"28","author":[{"given":"H G","family":"Brunner","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R M","family":"Winter","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1991,6,1]]},"reference":[{"key":"ref_1","first-page":"1","article-title":"Oesophageal atresia in the south-west of England. J7 Med","volume":"12","author":"David, T.J.; O'Caflaghan, S.E.","year":"1975","unstructured":"David TJ, O'Caflaghan SE. Oesophageal atresia in the south-west of England. J7 Med Genet 1975;12:1-11.","journal-title":"Genet"},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"51","DOI":"10.1007\/BF00389459","article-title":"Etiological study on isolated esophageal atresia","volume":"70","author":"Szendrey, T.; Danyi, G.; Czeizel, A.","year":"1985","unstructured":"Szendrey T, Danyi G, Czeizel A. Etiological study on isolated esophageal atresia. Hum Genet 1985;70:51-8.","journal-title":"Hum Genet"},{"issue":"5","key":"ref_3","first-page":"117","article-title":"Family studies on congenital esophageal atresia with or without tracheoesophageal fistula","volume":"15","author":"Chen, H.; Goei, G.S.; Hertzler, J.H.","year":"1979","unstructured":"Chen H, Goei GS, Hertzler JH. Family studies on congenital esophageal atresia with or without tracheoesophageal fistula. 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Hosp Pract 1978;13:44-9."},{"key":"ref_9","doi-asserted-by":"crossref","first-page":"491","DOI":"10.1136\/jmg.25.7.491","article-title":"Auralcephalosyndactyly: a new hereditary craniosynostosis","volume":"25","author":"Kurczynski, T.W.; Casperson, S.M.","year":"1988","unstructured":"Kurczynski TW, Casperson SM. Auralcephalosyndactyly: a new hereditary craniosynostosis. J Med Genet 1988;25:491-3.","journal-title":"J Med Genet"},{"key":"ref_10","first-page":"175","article-title":"Microcephaly: general considerations and aids to nosology","volume":"10","author":"Opitz, J.M.; Holt, M.C.","year":"1990","unstructured":"Opitz JM, Holt MC. Microcephaly: general considerations and aids to nosology. J Craniofac Genet Dev Biol 1990;10: 175-204.","journal-title":"J Craniofac Genet Dev Biol"},{"key":"ref_11","doi-asserted-by":"crossref","first-page":"442","DOI":"10.1002\/ajmg.1320340322","article-title":"Familial duodenal atresia: a report of two families and review","volume":"34","author":"Best, L.G.; Wiseman, N.E.; Chudley, A.E.","year":"1989","unstructured":"Best LG, Wiseman NE, Chudley AE. Familial duodenal atresia: a report of two families and review. Am J Med Genet 1989;34: 442-4.","journal-title":"Am J Med Genet"},{"key":"ref_12","article-title":"Catalogue of unbalanced chromosome aberrations in man","author":"Schinzel, A.","year":"1983","unstructured":"Schinzel A. Catalogue of unbalanced chromosome aberrations in man. 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