{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,11]],"date-time":"2026-05-11T11:28:37Z","timestamp":1778498917080,"version":"3.51.4"},"reference-count":28,"publisher":"BMJ","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[1976,10]]},"abstract":"<jats:p>A 43-year-old man is described who had Gardner's syndrome and steatocystoma multiplex. These two unusual genetically determined conditions were associated because he had inherited the Gardner's syndrome from his father and the steatocystoma multiplex from his mother.<\/jats:p>","DOI":"10.1136\/jmg.13.5.407","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T14:50:51Z","timestamp":1226328651000},"page":"407-411","source":"Crossref","is-referenced-by-count":4,"title":["Gardner's syndrome and steatocystoma multiplex. Two unusual genetically determined conditions occurring in same patient."],"prefix":"10.1136","volume":"13","author":[{"given":"B","family":"Leppard","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H R","family":"Thompson","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1976,10,1]]},"reference":[{"key":"ref_1","first-page":"660","article-title":"Gardner's syndrome","volume":"139","author":"Alm, T.; Dencker, H.; Lunderquist, A.; Mark, J.; Mitelman, F.; Norryd, C.; Tranberg, K.-G.","year":"1973","unstructured":"Alm, T., Dencker, H., Lunderquist, A., Mark, J., Mitelman, F., Norryd, C., and Tranberg, K-G. (1973). Gardner's syndrome. 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A genetic and clinical study of intestinal polyposis, a predisposing factor for carcinoma of the colon and rectum. American journal of Human Genetics, 3, 167-176.","journal-title":"American journal of Human Genetics"},{"key":"ref_8","first-page":"321","article-title":"Mendelian pattern of dominant inheritance for a syndrome including intestinal polyposis, oesteomas, fibromas and sebaceous cysts in a human family group. In Novant 'Anni Delle Leggi Mendeliane","volume-title":"Gedda. Instituto G. Mendel, Rome.","author":"Gardner, E.J.","year":"1956","unstructured":"Gardner, E. J. (1956). Mendelian pattern of dominant inheritance for a syndrome including intestinal polyposis, oesteomas, fibromas and sebaceous cysts in a human family group. In Novant 'Anni Delle Leggi Mendeliane, pp. 321-329. Ed. by L. Gedda. Instituto G. 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