{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,19]],"date-time":"2026-08-19T20:03:43Z","timestamp":1787169823997,"version":"build-2736575974"},"reference-count":14,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[1996,5,1]],"date-time":"1996-05-01T00:00:00Z","timestamp":830908800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Indian J Pediatr"],"published-print":{"date-parts":[[1996,5]]},"DOI":"10.1007\/bf02751537","type":"journal-article","created":{"date-parts":[[2007,11,17]],"date-time":"2007-11-17T22:45:52Z","timestamp":1195339552000},"page":"393-396","source":"Crossref","is-referenced-by-count":2,"title":["Partial trisomy 18q"],"prefix":"10.1007","volume":"63","author":[{"given":"M.","family":"Elbistan","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S.","family":"Kucukoduk","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"N.","family":"Kara","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","reference":[{"issue":"3","key":"BF02751537_CR1","doi-asserted-by":"crossref","first-page":"257","DOI":"10.1007\/BF01910544","volume":"36","author":"T Asano","year":"1991","unstructured":"Asano T, Ikeuchi T, Shinohara T, Enokido H, ashimoto K. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, (Review).Jap J Hum Genet 1991; 36 (3): 257\u2013265.","journal-title":"Jap J Hum Genet"},{"key":"BF02751537_CR2","doi-asserted-by":"crossref","first-page":"76","DOI":"10.1136\/jmg.15.1.76","volume":"15","author":"K Fried","year":"1978","unstructured":"Fried K, Bar-Yochal A, Rosenblatt M, Mundel G. Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation.J Med Genet 1978; 15: 76\u201378.","journal-title":"J Med Genet"},{"key":"BF02751537_CR3","doi-asserted-by":"crossref","first-page":"201","DOI":"10.1007\/BF00295415","volume":"44","author":"JP Fryns","year":"1978","unstructured":"Fryns JP, Detavernier F, Van Fleteren A, Van den Berghe H. Partial trisomy 18q in a newborn with typical 18 trisomy phenotype.Hum Genet 1978; 44: 201\u2013205.","journal-title":"Hum Genet"},{"key":"BF02751537_CR4","doi-asserted-by":"crossref","first-page":"341","DOI":"10.1007\/BF00273319","volume":"46","author":"JP Fryns","year":"1979","unstructured":"Fryns JP, Vinken L, Merien J, Van den Berghe H. Partial trisomy 18q12, due to intrachromosomal duplication, is not associated with typical 18 trisomy phenotype.Hum Genet 1979; 46: 341\u2013344.","journal-title":"Hum Genet"},{"key":"BF02751537_CR5","doi-asserted-by":"crossref","first-page":"78","DOI":"10.1007\/BF00271173","volume":"57","author":"R Matsuoka","year":"1981","unstructured":"Matsuoka R, Matsuyama S, Yamamoto Yet al. Trisomy 18q. A case report and review of karyotype-phenotype correlations.Hum Genet 1981; 57: 78\u201382.","journal-title":"Hum Genet"},{"issue":"6","key":"BF02751537_CR6","first-page":"1269","volume":"53","author":"R Mewar","year":"1993","unstructured":"Mewar R, Kline AD, Harrison Wet al. Clinical and molecular evaluation of four patients with partial duplications of the long arm of chromosome 18. (Review).Am J Hum Genet 1993; 53 (6): 1269\u20131278.","journal-title":"Am J Hum Genet"},{"key":"BF02751537_CR7","doi-asserted-by":"crossref","first-page":"520","DOI":"10.1136\/jmg.13.6.520","volume":"13","author":"RL Neu","year":"1976","unstructured":"Neu RL, Ortega CC, Barg GAet al. Inclusion of satellites in a 18\/21 translocation chromosome shown by ammoniacal-silver staining (sat-banding) in case of partial trisomy 18.J Med Genet 1976; 13: 520\u2013522.","journal-title":"J Med Genet"},{"issue":"10","key":"BF02751537_CR8","doi-asserted-by":"crossref","first-page":"983","DOI":"10.1002\/pd.1970131013","volume":"13","author":"E Pluchon","year":"1993","unstructured":"Pluchon E, Giovangrandi Y, Labbe Fet al. Prenatal diagnosis of a fetus with partial monosomy 7(q34 qter)and partial trisomy 18(q21 qter).Prenat Diagn 1993; 13 (10): 983\u2013988.","journal-title":"Prenat Diagn"},{"key":"BF02751537_CR9","doi-asserted-by":"crossref","first-page":"361","DOI":"10.1111\/j.1399-0004.1977.tb00955.x","volume":"12","author":"C Turleau","year":"1977","unstructured":"Turleau C, Grouchy J de. Trisomy 18qter and trisomy mapping of chromosome 18.Clin Genet 1977; 12: 361\u2013371.","journal-title":"Clin Genet"},{"issue":"4","key":"BF02751537_CR10","doi-asserted-by":"crossref","first-page":"506","DOI":"10.1002\/ajmg.1320360427","volume":"36","author":"GN Wilson","year":"1990","unstructured":"Wilson GN, Heller KB, Elterman RD, Schneider NR. Partial trisomy 18 with minimal anomalies: Lack of corresondence between phenotypic manifestations and triplicated loci along chromosome 18. (Review).Am J Med Genet 1990; 36 (4): 506\u2013510.","journal-title":"Am J Med Genet"},{"issue":"4","key":"BF02751537_CR11","first-page":"263","volume":"68","author":"R Vivarelli","year":"1992","unstructured":"Vivarelli R, Paolieri M, Anichini Cet al. Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18.Bull soc Ital Biol Sper 1992; 68 (4): 263\u2013269.","journal-title":"Bull soc Ital Biol Sper"},{"issue":"5","key":"BF02751537_CR12","doi-asserted-by":"crossref","first-page":"520","DOI":"10.1002\/ajmg.1320460512","volume":"46","author":"DJ Wolf","year":"1993","unstructured":"Wolf DJ, Schwartz MF, Cohen MM, Schwartz S. Precise mapping of a de novo duplication 18 (q21 q22) utilizing cytogenetic, biochemical and molecular techniques.Am J Med Genet 1993; 46 (5): 520\u2013523.","journal-title":"Am J Med Genet"},{"key":"BF02751537_CR13","doi-asserted-by":"crossref","unstructured":"Moorhead PS, Nowell PC, Mellman WJet al. Chromosome preparations of leucocytes cultured from peripheral blood.Exp Cell Res 1960; 613\u2013616.","DOI":"10.1016\/0014-4827(60)90138-5"},{"key":"BF02751537_CR14","first-page":"45","volume-title":"Human Chromosomes: Manual of Basic Techniques","author":"RS Verma","year":"1989","unstructured":"Verma RS, Babu A.Human Chromosomes: Manual of Basic Techniques. New York: Pergamon Press, 1989; 45\u2013114."}],"container-title":["The Indian Journal of Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02751537.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF02751537\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02751537","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,21]],"date-time":"2019-05-21T11:38:56Z","timestamp":1558438736000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF02751537"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1996,5]]},"references-count":14,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1996,5]]}},"alternative-id":["BF02751537"],"URL":"https:\/\/doi.org\/10.1007\/bf02751537","relation":{},"ISSN":["0019-5456","0973-7693"],"issn-type":[{"value":"0019-5456","type":"print"},{"value":"0973-7693","type":"electronic"}],"subject":[],"published":{"date-parts":[[1996,5]]}}}