{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,18]],"date-time":"2025-10-18T05:10:07Z","timestamp":1760764207880,"version":"build-2065373602"},"reference-count":19,"publisher":"BMJ","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[1982,8]]},"abstract":"<jats:p>The Poland anomaly is usually a non-genetic malformation syndrome. This paper reports two second cousins who both had a typical left sided Poland anomaly, and this constitutes the first recorded case of this condition affecting more than one member of a family. Despite this, for the purposes of genetic counselling, the Poland anomaly can be regarded as a sporadic condition with an extremely low recurrence risk.<\/jats:p>","DOI":"10.1136\/jmg.19.4.293","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T14:52:06Z","timestamp":1226328726000},"page":"293-296","source":"Crossref","is-referenced-by-count":46,"title":["Familial Poland anomaly."],"prefix":"10.1136","volume":"19","author":[{"given":"T J","family":"David","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1982,8,1]]},"reference":[{"key":"ref_1","first-page":"52","article-title":"Poland's syndrome. A review of forty-three cases","volume":"58","author":"Ireland, D.C.; Takayama, N.; Flatt, A.E.","year":"1976","unstructured":"Ireland DC, Takayama N, Flatt AE. Poland's syndrome. A review of forty-three cases. 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