{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,21]],"date-time":"2025-10-21T15:01:03Z","timestamp":1761058863008,"version":"build-2065373602"},"reference-count":14,"publisher":"BMJ","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[1980,2]]},"abstract":"<jats:p>The clinical and radiographic manifestations in a 45-year-old male with frontometaphyseal dysplasia (FMD) are documented and depicted. Deafness and degenerative osteoarthropathy in weight-bearing joints were the main clinical problems. Widespread patchy cranial sclerosis was reminiscent of Paget's disease, while digital deformity resembled rheumatoid arthritis. On the basis of a review and tabulation of published reports, evidence emerges to support the concept of X-linked inheritance. The relationship between FMD and osteodysplasty remains a matter for speculation.<\/jats:p>","DOI":"10.1136\/jmg.17.1.53","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T14:52:06Z","timestamp":1226328726000},"page":"53-56","source":"Crossref","is-referenced-by-count":25,"title":["Frontometaphyseal dysplasia: autosomal dominant or X-linked?"],"prefix":"10.1136","volume":"17","author":[{"given":"P","family":"Beighton","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H","family":"Hamersma","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1980,2,1]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"487","DOI":"10.1001\/archpedi.1969.02100040489014","article-title":"Frontometaphyseal dysplasia","volume":"118","author":"Gorlin, R.J.; Cohen, M.M.","year":"1969","unstructured":"Gorlin RJ, Cohen MM. 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