{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,11]],"date-time":"2026-03-11T23:07:05Z","timestamp":1773270425546,"version":"3.50.1"},"reference-count":22,"publisher":"BMJ","issue":"10","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[2000,10,1]]},"DOI":"10.1136\/jmg.37.10.787","type":"journal-article","created":{"date-parts":[[2002,7,27]],"date-time":"2002-07-27T06:33:18Z","timestamp":1027751598000},"page":"787-789","source":"Crossref","is-referenced-by-count":21,"title":["Hemiplegic cerebral palsy and the factor V Leiden mutation: Table 1"],"prefix":"10.1136","volume":"37","author":[{"given":"J L","family":"HALLIDAY","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D","family":"REDDIHOUGH","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"K","family":"BYRON","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H","family":"EKERT","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M","family":"DITCHFIELD","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2000,10,1]]},"reference":[{"key":"2025101715233327000_37.10.787.1","doi-asserted-by":"publisher","DOI":"10.1038\/369064a0"},{"key":"2025101715233327000_37.10.787.2","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(94)92940-8"},{"key":"2025101715233327000_37.10.787.3","doi-asserted-by":"publisher","DOI":"10.1073\/pnas.90.3.1004"},{"key":"2025101715233327000_37.10.787.4","doi-asserted-by":"crossref","first-page":"3698","DOI":"10.1182\/blood.V88.10.3698.bloodjournal88103698","article-title":"A common genetic variation in the 3\u2032-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.","volume":"88","author":"Poort","year":"1996","journal-title":"Blood"},{"key":"2025101715233327000_37.10.787.5","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1177\/107602969700300213","article-title":"Prevalence of factor V Leiden is not increased in women with recurrent miscarriage.","volume":"3","author":"Metz","year":"1997","journal-title":"Clin Appl Thromb\/Hemo"},{"key":"2025101715233327000_37.10.787.6","doi-asserted-by":"crossref","first-page":"491","DOI":"10.1097\/00001721-199711000-00002","article-title":"Use of first nucleotide change technology to determine the frequency of factor V Leiden in a population of Australian blood donors.","volume":"8","author":"Pecheniuk","year":"1997","journal-title":"Blood Coag Fibrin"},{"key":"2025101715233327000_37.10.787.7","doi-asserted-by":"crossref","first-page":"684","DOI":"10.1097\/00001721-199610000-00004","article-title":"Ischaemic stroke in infancy and childhood: role of the Arg506 to Gln mutation in the factor V gene.","volume":"7","author":"Nowak-Gottl","year":"1996","journal-title":"Blood Coag Fibrin"},{"key":"2025101715233327000_37.10.787.8","doi-asserted-by":"crossref","first-page":"260","DOI":"10.1016\/S0140-6736(96)90434-1","article-title":"Activated protein C resistance in childhood stroke.","volume":"347","author":"Ganesan","year":"1996","journal-title":"Lancet"},{"key":"2025101715233327000_37.10.787.9","doi-asserted-by":"crossref","first-page":"763","DOI":"10.1055\/s-0037-1615355","article-title":"Factor V Leiden and prothrombin gene G 20210 a variant in children with ischemic stroke.","volume":"80","author":"Zenz","year":"1998","journal-title":"Thromb Haemostas"},{"key":"2025101715233327000_37.10.787.10","doi-asserted-by":"publisher","DOI":"10.1007\/s004310050523"},{"key":"2025101715233327000_37.10.787.11","doi-asserted-by":"publisher","DOI":"10.1007\/s004310050877"},{"key":"2025101715233327000_37.10.787.12","doi-asserted-by":"crossref","first-page":"690","DOI":"10.1055\/s-0037-1614555","article-title":"Factor V Leiden, prothrombin 20210 G\u2192A and the MTHFR C677T mutations in childhood stroke.","volume":"81","author":"McColl","year":"1999","journal-title":"Thromb Haemostas"},{"key":"2025101715233327000_37.10.787.13","doi-asserted-by":"publisher","DOI":"10.1002\/ana.410420316"},{"key":"2025101715233327000_37.10.787.14","doi-asserted-by":"crossref","first-page":"489","DOI":"10.1046\/j.1365-2141.0000.d01-1465.x","article-title":"Second-trimester pregnancy loss with activated protein C resistance.","volume":"92","author":"Rai","year":"1996","journal-title":"Br J Haematol"},{"key":"2025101715233327000_37.10.787.15","doi-asserted-by":"crossref","first-page":"822","DOI":"10.1055\/s-0038-1656060","article-title":"Factor V Leiden is associated with repeated and recurrent unexplained fetal losses.","volume":"77","author":"Grandone","year":"1997","journal-title":"Thromb Haemostas"},{"key":"2025101715233327000_37.10.787.16","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(88)80161-6"},{"key":"2025101715233327000_37.10.787.17","doi-asserted-by":"publisher","DOI":"10.1001\/archpedi.1989.02150220044018"},{"key":"2025101715233327000_37.10.787.18","doi-asserted-by":"crossref","first-page":"156","DOI":"10.1111\/j.1365-3016.1995.tb00131.x","article-title":"Assessing the contribution of birth asphyxia to cerebral palsy in term singletons.","volume":"9","author":"Yudkin","year":"1995","journal-title":"Paediatr Perinat Epidemiol"},{"key":"2025101715233327000_37.10.787.19","doi-asserted-by":"publisher","DOI":"10.1001\/jama.1982.03320350071039"},{"key":"2025101715233327000_37.10.787.20","doi-asserted-by":"publisher","DOI":"10.1136\/adc.64.7.1013"},{"key":"2025101715233327000_37.10.787.21","doi-asserted-by":"publisher","DOI":"10.1016\/S0002-9378(96)80022-6"},{"key":"2025101715233327000_37.10.787.22","doi-asserted-by":"crossref","first-page":"1062","DOI":"10.1093\/oxfordjournals.aje.a009400","article-title":"Comparison of risk factors for preeclampsia and gestational hypertension in a population-based cohort study.","volume":"147","author":"Ros","year":"1998","journal-title":"Am J Epidemiol"}],"container-title":["Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jmg.37.10.787","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,10,17]],"date-time":"2025-10-17T22:23:45Z","timestamp":1760739825000},"score":1,"resource":{"primary":{"URL":"https:\/\/jmg.bmj.com\/lookup\/doi\/10.1136\/jmg.37.10.787"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2000,10,1]]},"references-count":22,"journal-issue":{"issue":"10","published-online":{"date-parts":[[2000,10,1]]},"published-print":{"date-parts":[[2000,10,1]]}},"alternative-id":["10.1136\/jmg.37.10.787"],"URL":"https:\/\/doi.org\/10.1136\/jmg.37.10.787","relation":{},"ISSN":["0022-2593","1468-6244"],"issn-type":[{"value":"0022-2593","type":"print"},{"value":"1468-6244","type":"electronic"}],"subject":[],"published":{"date-parts":[[2000,10,1]]}}}