{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T14:26:58Z","timestamp":1786976818148,"version":"build-2736575974"},"reference-count":13,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2005,6,3]],"date-time":"2005-06-03T00:00:00Z","timestamp":1117756800000},"content-version":"vor","delay-in-days":6303,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1988,3]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>The Weismann\u2010Netter syndrome is a rare, heritable dysplasia of anterior bowing of tibiae and fibulae, often with lateral bowing of femora, short stature, and mild mental retardation. The condition is probably due to a primary metabolic abnormality of bone. The disease process is inactive in the adult. The pathogenesis is unknown. The patient reported here is the only child described in the Anglo\u2010American literature.<\/jats:p>","DOI":"10.1002\/ajmg.1320290315","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T23:06:26Z","timestamp":1118531186000},"page":"573-579","source":"Crossref","is-referenced-by-count":16,"title":["The Weismann\u2010Netter syndrome"],"prefix":"10.1002","volume":"29","author":[{"given":"Meinhard","family":"Robinow","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"G. 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