{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,18]],"date-time":"2025-10-18T07:10:59Z","timestamp":1760771459477,"version":"build-2065373602"},"reference-count":13,"publisher":"BMJ","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[1982,4]]},"abstract":"<jats:p>Partial deletion of the long arm of chromosome 4 at q31 results in a clinical syndrome of mental retardation, characteristic ears, facial bone hypoplasia, cleft palate very prone to scarring on repair, and specific hand abnormalities. A female, aged 9 years, is described and compared with six other reported cases.<\/jats:p>","DOI":"10.1136\/jmg.19.2.155","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T14:52:06Z","timestamp":1226328726000},"page":"155-157","source":"Crossref","is-referenced-by-count":8,"title":["Partial deletion of the long arm of chromosome 4: a clinical syndrome"],"prefix":"10.1136","volume":"19","author":[{"given":"A","family":"Lipson","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J","family":"Collist","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C","family":"Green","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[1982,4,1]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"111","DOI":"10.1159\/000153026","article-title":"Pericentric inversions of chromosome number 9: benign or harmful","volume":"29","author":"Howard-Peebles, P.N.; Stoddard, G.R.","year":"1979","unstructured":"Howard-Peebles PN, Stoddard GR. 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Bull Eur Soc Hum Genet 1973:46-8.","journal-title":"Bull Eur Soc Hum Genet"},{"key":"ref_6","first-page":"402","article-title":"Study on segregation and risk for abnormal offspring in carriers of pericentric inversion of the (pl lql3) segment of chromosome 2. Clin Genet","volume":"18","author":"Baccichetti, C.; Lenzini, E.; Peserico, A.; Tenconi, R.","year":"1980","unstructured":"Baccichetti C, Lenzini E, Peserico A, Tenconi R. Study on segregation and risk for abnormal offspring in carriers of pericentric inversion of the (pl lql3) segment of chromosome 2. Clin Genet 1980;18:402-7."},{"key":"ref_7","article-title":"Case report The proband is the 9-year-old daughter of a 30-yearold father and 25-year-old mother. The parents are FIG 2 The proband. Note small jaw, facial bone Received for publication","volume-title":"hypoplasia, and prominent ears","year":"1981","unstructured":"Case report The proband is the 9-year-old daughter of a 30-yearold father and 25-year-old mother. The parents are FIG 2 The proband. Note small jaw, facial bone Received for publication 24 June 1981 hypoplasia, and prominent ears."},{"key":"ref_8","doi-asserted-by":"crossref","first-page":"971","DOI":"10.1016\/S0140-6736(71)90287-X","article-title":"A rapid banding technique for human chromosomes","volume":"ii:","author":"Seabright, M.","year":"1971","unstructured":"Seabright M. A rapid banding technique for human chromosomes. Lancet 1971;ii:971-2.","journal-title":"Lancet"},{"key":"ref_9","first-page":"383","article-title":"4q-syndrome","volume":"133","author":"Townes, P.L.; White, M.; Marzo, G.V.","year":"1979","unstructured":"Townes PL, White M, Marzo GV. 4q-syndrome. 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