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These observations may prove helpful in the search for better genetic markers for Huntington's chorea, which maps close to D4S10.<\/jats:p>","DOI":"10.1136\/jmg.24.7.410","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:09:16Z","timestamp":1226329756000},"page":"410-412","source":"Crossref","is-referenced-by-count":21,"title":["Wolf-Hirschhorn locus is distal to D4S10 on short arm of chromosome 4."],"prefix":"10.1136","volume":"24","author":[{"given":"C","family":"McKeown","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A P","family":"Read","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A","family":"Dodge","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"O","family":"Stecko","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A","family":"Mercer","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R","family":"Harris","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1987,7,1]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"234","DOI":"10.1038\/306234a0","article-title":"A polymorphic DNA marker genetically linked to Huntington's disease","volume":"306","author":"Gusella, J.F.; Wexler, N.S.; Conneally, P.M.","year":"1983","unstructured":"Gusella JF, Wexler NS, Conneally PM, et al. A polymorphic DNA marker genetically linked to Huntington's disease. Nature 1983;306:234-8.","journal-title":"Nature"},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1038\/318075a0","article-title":"Deletion of Huntington's disease-linked G8 (D4S1() locus in Wolf-Hirschhorn syndrome","volume":"318","author":"Gusella, J.F.; Tanzi, R.E.; Bader, P.I.","year":"1985","unstructured":"Gusella JF, Tanzi RE, Bader PI, et al. Deletion of Huntington's disease-linked G8 (D4S1() locus in Wolf-Hirschhorn syndrome. Nature 1985;318:75-8.","journal-title":"Nature"},{"key":"ref_3","first-page":"500","article-title":"Familial Wolf's syndrome with a hidden 4p deletion by translocation of an 8p segment. Unbalanced inheritance from a maternal translocation","volume":"25","author":"Stengel-Rutkowski, S.; Warkotsch, A.; Schimanek, P.; Stene, J.","year":"1984","unstructured":"Stengel-Rutkowski S, Warkotsch A, Schimanek P, Stene J. Familial Wolf's syndrome with a hidden 4p deletion by translocation of an 8p segment. Unbalanced inheritance from a maternal translocation (4;8) (pl5-3;p22). Case report, review and risk estimates. Clin Genet 1984;25:500-21.","journal-title":"Clin Genet; Case report, review and risk estimates"},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"297","DOI":"10.1007\/BF00295461","article-title":"Genetic and clinical studies in 13 patients with the WolfHirschhorn syndrome ldel(4)l","volume":"59","author":"Wilson, M.G.; Towner, J.W.; Coffin, G.S.; Ebbin, A.J.; Siris, E.; Brager, P.","year":"1981","unstructured":"Wilson MG, Towner JW, Coffin GS, Ebbin AJ, Siris E, Brager P. Genetic and clinical studies in 13 patients with the WolfHirschhorn syndrome ldel(4)l. Hum Genet 1981;59:297-3t)7.","journal-title":"Hum Genet"},{"key":"ref_5","first-page":"458","article-title":"Catalogue of unbalanced chromosomne aberration.s in man","author":"Schinzel, A.","year":"1984","unstructured":"Schinzel A. Catalogue of unbalanced chromosomne aberration.s in man. Berlin: Walter de Gruyter, 1984:458-61."},{"key":"ref_6","doi-asserted-by":"crossref","first-page":"4778","DOI":"10.1073\/pnas.82.14.4778","article-title":"Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion","volume":"82","author":"Kunkel, L.M.; Monaco, A.P.; Middlesworth, W.; Ochs, H.D.; Latt, S.A.","year":"1985","unstructured":"Kunkel LM, Monaco AP, Middlesworth W, Ochs HD, Latt SA. Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. Proc NatI Acad Sci USA 1985;82:4778-82.","journal-title":"Proc NatI Acad Sci USA"}],"container-title":["Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jmg.24.7.410","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,10,6]],"date-time":"2025-10-06T04:07:01Z","timestamp":1759723621000},"score":1,"resource":{"primary":{"URL":"https:\/\/jmg.bmj.com\/lookup\/doi\/10.1136\/jmg.24.7.410"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1987,7]]},"references-count":6,"journal-issue":{"issue":"7","published-online":{"date-parts":[[1987,7,1]]},"published-print":{"date-parts":[[1987,7]]}},"alternative-id":["10.1136\/jmg.24.7.410"],"URL":"https:\/\/doi.org\/10.1136\/jmg.24.7.410","relation":{},"ISSN":["0022-2593","1468-6244"],"issn-type":[{"value":"0022-2593","type":"print"},{"value":"1468-6244","type":"electronic"}],"subject":[],"published":{"date-parts":[[1987,7]]}}}