{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,4]],"date-time":"2026-10-04T20:29:50Z","timestamp":1791145790793,"version":"4.1.0"},"reference-count":11,"publisher":"BMJ","issue":"10","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[1995,10]]},"abstract":"<jats:p>The WAGR syndrome (Wilms' tumour, aniridia, genital anomalies, and mental retardation) is well documented to be associated with a deletion of 11p13. We present a patient with a del(11)(p11.2p14.2) who as well as all the features of WAGR syndrome has multiple exostoses. We suggest that this could be a possible locus for hereditary multiple exostoses.<\/jats:p>","DOI":"10.1136\/jmg.32.10.823","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:23:16Z","timestamp":1226330596000},"page":"823-824","source":"Crossref","is-referenced-by-count":26,"title":["WAGR syndrome and multiple exostoses in a patient with del(11)(p11.2p14.2)"],"prefix":"10.1136","volume":"32","author":[{"given":"J M","family":"McGaughran","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H B","family":"Ward","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D G R","family":"Evans","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","published-online":{"date-parts":[[1995,10,1]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"922","DOI":"10.1056\/NEJM196404302701802","article-title":"Association of Wilm's tumour with aniridia, hemihypertrophy and other congenital malformations","volume":"270","year":"1964","unstructured":"Miller RW, Fraumeni JF Jr, Manning MD. Association of Wilm's tumour with aniridia, hemihypertrophy and other congenital malformations. N EnglJ Med 1964;270:922-7.","journal-title":"N EnglJ Med"},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"182","DOI":"10.1002\/mpo.2950210306","article-title":"Clinical phenotypes and Wilms tumour","volume":"21","author":"Clericuzio, C.L.","year":"1993","unstructured":"Clericuzio CL. Clinical phenotypes and Wilms tumour. Med Paediatr Oncol 1993;21:182-7.","journal-title":"Med Paediatr Oncol"},{"key":"ref_3","first-page":"255","article-title":"Obesity: a new feature of WAGR (del lip) syndrome","volume":"3","author":"Marlin, S.; Couet, D.; Lacombe, D.; Cessans, C.; Bonneau, D.","year":"1994","unstructured":"Marlin S, Couet D, Lacombe D, Cessans C, Bonneau D. Obesity: a new feature of WAGR (del lip) syndrome. 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Genetic heterogeneity in families with hereditary multiple exostoses","volume":"53","author":"Cook, A.; Raskind, W.","year":"1993","unstructured":"Cook A, Raskind W, Blanton SH, et al. Genetic heterogeneity in families with hereditary multiple exostoses. Am JrHum Genet 1993;53:71-9.","journal-title":"Am JrHum Genet"},{"key":"ref_9","doi-asserted-by":"crossref","first-page":"881","DOI":"10.1136\/jmg.28.12.881","article-title":"Multiple exostoses in a patient with t(8; I1)(q24. I1; pi5.5)","volume":"28","author":"Ogle, R.F.; Dalzell, P.; Turner, G.; Wass, D.; Yip, M.-Y.","year":"1991","unstructured":"Ogle RF, Dalzell P, Turner G, Wass D, Yip M-Y Multiple exostoses in a patient with t(8;I1)(q24.I1;pi5.5). JMed Genet 1991;28:881-3.","journal-title":"JMed Genet"},{"key":"ref_10","doi-asserted-by":"crossref","first-page":"167","DOI":"10.1093\/hmg\/3.1.167","article-title":"Assignment of a second locus for multiple exostoses to the pericentromeric region ofchromosome 11","volume":"3","author":"Wu, Y.Q.; Heutink, P.; de Vries, B.B.A.","year":"1994","unstructured":"Wu YQ, Heutink P, de Vries BBA, et al. Assignment of a second locus for multiple exostoses to the pericentromeric region ofchromosome 11. Hum Mol Genet 1994;3: 167-71.","journal-title":"Hum Mol Genet"},{"key":"ref_11","doi-asserted-by":"crossref","first-page":"717","DOI":"10.1093\/hmg\/3.5.717","article-title":"A gene for hereditary multiple exostoses maps to chromosome 19p","volume":"3","author":"M, Le Merrer; L, Legeai-Mallet; PM, Jeannin","year":"1994","unstructured":"Le Merrer M, Legeai-Mallet L, Jeannin PM, et al. A gene for hereditary multiple exostoses maps to chromosome 19p. 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