{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,6,5]],"date-time":"2025-06-05T08:49:00Z","timestamp":1749113340918},"reference-count":27,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[1995,2,1]],"date-time":"1995-02-01T00:00:00Z","timestamp":791596800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Autism Dev Disord"],"published-print":{"date-parts":[[1995,2]]},"DOI":"10.1007\/bf02178166","type":"journal-article","created":{"date-parts":[[2005,9,20]],"date-time":"2005-09-20T20:48:21Z","timestamp":1127249301000},"page":"41-49","source":"Crossref","is-referenced-by-count":32,"title":["A case of autism associated with partial tetrasomy 15"],"prefix":"10.1007","volume":"25","author":[{"given":"Matthew","family":"Hotopf","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Patrick","family":"Bolton","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"BF02178166_CR1","doi-asserted-by":"crossref","first-page":"737","DOI":"10.1111\/j.1469-8749.1991.tb14953.x","volume":"33","author":"A. \u00c5kefeldt","year":"1991","unstructured":"\u00c5kefeldt, A., & Gillberg, C. (1991). Hypomelanosis of Ito in three cases with autism and autism-like conditions.Developmental Medicine and Child Neurology, 33, 737\u2013743.","journal-title":"Developmental Medicine and Child Neurology"},{"key":"BF02178166_CR2","doi-asserted-by":"crossref","first-page":"672","DOI":"10.1111\/j.1469-7610.1993.tb01064.x","volume":"34","author":"A. Bailey","year":"1993","unstructured":"Bailey, A., Bolton, P., Butler, L., Le Couteur, A., Murphy, M., Scott, S., Webb, T., & Rutter, M. (1993). Prevalence of fragile X anomaly amongst autistic twins and singletons.Journal of Child Psychology and Psychiatry, 34, 672\u2013688.","journal-title":"Journal of Child Psychology and Psychiatry"},{"key":"BF02178166_CR3","doi-asserted-by":"crossref","unstructured":"Bailey, A., Le Couteur, A., Gottesman, I., Bolton, P., Simonoff, E., Yuzda, E., & Rutter, M. (in press). Autism as a strongly genetic disorder: evidence from a British twin study.Psychological Medicine.","DOI":"10.1017\/S0033291700028099"},{"key":"BF02178166_CR4","volume-title":"Child and adolescent psychiatry: Modern approaches","author":"P. Bolton","year":"1994","unstructured":"Bolton, P., & Holland, A. (1994). Chromosomal abnormalities. In M. Rutter, E. Taylor, & L. Hersov (Eds.),Child and adolescent psychiatry: Modern approaches. London: Blackwell."},{"key":"BF02178166_CR5","doi-asserted-by":"crossref","first-page":"877","DOI":"10.1111\/j.1469-7610.1994.tb02300.x","volume":"35","author":"P. Bolton","year":"1994","unstructured":"Bolton, P., Macdonald, H., Pickles, A., Rios, P., Goode, S., Crowson, M., Bailey, A., & Rutter, M. (1994). A case control family history study of autism.Journal of Child Psychology and Psychiatry.35, 877\u2013900.","journal-title":"Journal of Child Psychology and Psychiatry"},{"key":"BF02178166_CR6","first-page":"174","volume":"3","author":"P. Bolton","year":"1993","unstructured":"Bolton, P., Murphy, M., Sim, L., & Rutter, M. (1993). Obstetric complications in autism.Psychiatric Genetics, 3, 174.","journal-title":"Psychiatric Genetics"},{"key":"BF02178166_CR7","doi-asserted-by":"crossref","first-page":"277","DOI":"10.1097\/00041444-199210000-00005","volume":"2","author":"P. Bolton","year":"1992","unstructured":"Bolton, P., Pickles, A., Butler, L., Summers, D., Webb, T., Lord, C., Le Couteur, A., Bailey, A., & Rutter, M. (1992). Fragile X in families multiplex for autism and related phenotypes: prevalence and criteria for cytogenetic diagnosis.Psychiatric Genetics, 2, 277\u2013300.","journal-title":"Psychiatric Genetics"},{"key":"BF02178166_CR8","doi-asserted-by":"crossref","first-page":"67","DOI":"10.3109\/09540269009028273","volume":"2","author":"P. Bolton","year":"1990","unstructured":"Bolton, P., & Rutter, M. (1990). Genetic influences in autism.International Review of Psychiatry, 2, 67\u201380.","journal-title":"International Review of Psychiatry"},{"key":"BF02178166_CR9","doi-asserted-by":"crossref","first-page":"442","DOI":"10.1159\/000152759","volume":"25","author":"W. Centerall","year":"1975","unstructured":"Centerall, W., & Morris, J. (1975). Partial D trisomy 15.Human Heredity, 25, 442\u2013452.","journal-title":"Human Heredity"},{"key":"BF02178166_CR10","doi-asserted-by":"crossref","first-page":"529","DOI":"10.1136\/jmg.30.6.529","volume":"30","author":"J. Clayton-Smith","year":"1993","unstructured":"Clayton-Smith, J., Webb, T., Cheng, X. J., Pembry, M. E., & Malcolm, S. (1993). Duplication of chromosome 15 in the region 15q11\u201313 in a patient with developmental delay and ataxia with similarities to Angelman syndrome.Journal of Medical Genetics, 30, 529\u2013531.","journal-title":"Journal of Medical Genetics"},{"key":"BF02178166_CR11","doi-asserted-by":"crossref","first-page":"213","DOI":"10.1136\/jmg.21.3.213","volume":"21","author":"J. M. Connor","year":"1984","unstructured":"Connor, J. M., & Gilmore, D. H. (1984). An analysis of the parental age effect for invdup(15).Journal of Medical Genetics, 21, 213\u2013214.","journal-title":"Journal of Medical Genetics"},{"key":"BF02178166_CR12","doi-asserted-by":"crossref","first-page":"563","DOI":"10.1007\/BF01046328","volume":"22","author":"E. Fombonne","year":"1992","unstructured":"Fombonne, E. (1992). Diagnostic assessment in a sample of autistic and developmentally impaired adolescents.Journal of Autism and Developmental Disorders, 22, 563\u2013581.","journal-title":"Journal of Autism and Developmental Disorders"},{"key":"BF02178166_CR13","doi-asserted-by":"crossref","first-page":"489","DOI":"10.1097\/00004583-199105000-00022","volume":"30","author":"C. Gillberg","year":"1991","unstructured":"Gillberg, C., Steffenburg, S., Wahlstr\u00f6m, J., Gillberg, I., Sj\u00f6sted, A., Martinsson, T., Liedgren, S., & Eeg-Olofsson, O. (1991). Autism associated with marker chromosome.Journal of the American Academy of Child and Adolescent Psychiatry, 30, 489\u2013494.","journal-title":"Journal of the American Academy of Child and Adolescent Psychiatry"},{"key":"BF02178166_CR14","doi-asserted-by":"crossref","first-page":"221","DOI":"10.1136\/jmg.21.3.221","volume":"21","author":"D. H. Gilmore","year":"1984","unstructured":"Gilmore, D. H., Boyd, E., McClure, J. P., Batstone, P., & Connor, J. M. (1984). Inv Dup (15) with mental retardation but few dysmorphic features.Journal of Medical Genetics, 21, 221\u2013223.","journal-title":"Journal of Medical Genetics"},{"key":"BF02178166_CR15","doi-asserted-by":"crossref","first-page":"363","DOI":"10.1007\/BF02212936","volume":"19","author":"A. Couteur Le","year":"1989","unstructured":"Le Couteur, A., Rutter, M., Lord, C., Rios, P., Robertson, S., Holgafer, M., & McLennan, J. (1989). Autism diagnostic interview: a standardized investigator based instrument.Journal of Autism and Developmental Disorders, 19, 363\u2013387.","journal-title":"Journal of Autism and Developmental Disorders"},{"key":"BF02178166_CR16","first-page":"615","volume-title":"The cytogenetics of mammalian autosomal rearrangements","author":"P. Maraschio","year":"1988","unstructured":"Maraschio, P., Cuoco, G., Gimelli, G., Zuffardi, O., & Tiepolo, L. (1988). Origin and clinical significance of inv dup(15). In D. Art (Ed.),The cytogenetics of mammalian autosomal rearrangements (pp. 615\u2013634). New York: Liss."},{"key":"BF02178166_CR17","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1136\/jmg.30.1.1","volume":"30","author":"V. McKusick","year":"1993","unstructured":"McKusick, V., & Amberger, J. (1993). The morbid anatomy of the human genome: chromosomal location of mutations causing disease.Journal of Medical Genetics, 30, 1\u201326.","journal-title":"Journal of Medical Genetics"},{"key":"BF02178166_CR18","doi-asserted-by":"crossref","first-page":"1073","DOI":"10.1016\/S0140-6736(72)91259-7","volume":"1","author":"C. E. Parker","year":"1972","unstructured":"Parker, C. E., & Alfi, O. S. (1972). Partial trisomy of chromosome 15.Lancet, 1, 1073.","journal-title":"Lancet"},{"key":"BF02178166_CR19","first-page":"825","volume":"30","author":"J. Piven","year":"1991","unstructured":"Piven, J., Gayle, J., Landa, R., Wzorek, M., & Folstein, S. (1991). The prevalence of Fragile X in a sample of autistic individuals diagnosed using a standardized interview.Journal of American Academy of Child and Adolescent Psychiatry, 30, 825\u2013830.","journal-title":"Journal of American Academy of Child and Adolescent Psychiatry"},{"key":"BF02178166_CR20","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1159\/000472386","volume":"1","author":"W. P. Robinson","year":"1993","unstructured":"Robinson, W. P., Binkert, F., Gin\u00e9, R., Vazquez, C., M\u00fcller, W., Rosenkranz, W., & Schinzel, A. (1993a). Clinical and molecular analysis of five inv dup(15) patients.European Journal of Human Genetics, 1, 37\u201350.","journal-title":"European Journal of Human Genetics"},{"key":"BF02178166_CR21","doi-asserted-by":"crossref","first-page":"756","DOI":"10.1136\/jmg.30.9.756","volume":"30","author":"W. P. Robinson","year":"1993","unstructured":"Robinson, W. P., Wagstaff, J., Bernasconi, F., Baccichetti, C., Artifoni, L., Franzoni, E., Suslak, L., Shih, L-Y., Aviv, H., & Schinzel, A. (1993b). Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.Journal of Medical Genetics, 30, 756\u2013760.","journal-title":"Journal of Medical Genetics"},{"key":"BF02178166_CR22","doi-asserted-by":"crossref","first-page":"311","DOI":"10.1111\/j.1469-7610.1994.tb01164.x","volume":"35","author":"M. Rutter","year":"1994","unstructured":"Rutter, M., Bailey, A., Bolton, P., & Le Couteur, A. (1994). Medical disorders in autism: Myth and substance.Journal of Child Psychology and Psychiatry, 35, 311\u2013322.","journal-title":"Journal of Child Psychology and Psychiatry"},{"key":"BF02178166_CR23","volume-title":"Human behaviour and genetics","author":"A. Schinzel","year":"1981","unstructured":"Schinzel, A. (1981). Particular behavioral symptomatology in patients with rare autosomal chromosome aberrations. In W. Schmid & J. Nielsen (Eds.),Human behaviour and genetics. Amsterdam: Elsevier, North Holland."},{"key":"BF02178166_CR24","first-page":"180","volume-title":"Neurobiological issues in autism","author":"L. Tsai","year":"1987","unstructured":"Tsai, L. (1987). Pre-, peri-, neo-natal factors in autism. In E. Schopler & G. B. Mesibov (Eds.),Neurobiological issues in autism (pp. 180\u2013189). New York: Plenum Press."},{"key":"BF02178166_CR25","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1192\/bjp.156.1.17","volume":"156","author":"M. Tsuang","year":"1990","unstructured":"Tsuang, M., Lyons, M., & Faraone, S. (1990). Heterogeneity of schizophrenia: conceptual models and analytic strategies.British Journal of Psychiatry, 156, 17\u201326.","journal-title":"British Journal of Psychiatry"},{"key":"BF02178166_CR26","doi-asserted-by":"crossref","first-page":"259","DOI":"10.1007\/BF00399391","volume":"50","author":"L. Wisniewski","year":"1979","unstructured":"Wisniewski, L., Hassold, T., Heffelfinger, J., & Higgins, J. V. (1979). Cytogenetic and clinical studies in 5 cases of Inv Dup (15).Human Genetics, 50, 259\u2013270.","journal-title":"Human Genetics"},{"key":"BF02178166_CR27","doi-asserted-by":"crossref","first-page":"170","DOI":"10.1007\/BF02091902","volume":"1","author":"M. Zapella","year":"1992","unstructured":"Zapella, M. (1992). Hypomelanosis of Ito is frequently associated with autism.European Child and Adolescent Psychiatry, 1, 170\u2013177.","journal-title":"European Child and Adolescent Psychiatry"}],"container-title":["Journal of Autism and Developmental Disorders"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02178166.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF02178166\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02178166","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,15]],"date-time":"2019-05-15T12:32:00Z","timestamp":1557923520000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF02178166"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1995,2]]},"references-count":27,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1995,2]]}},"alternative-id":["BF02178166"],"URL":"https:\/\/doi.org\/10.1007\/bf02178166","relation":{},"ISSN":["0162-3257","1573-3432"],"issn-type":[{"value":"0162-3257","type":"print"},{"value":"1573-3432","type":"electronic"}],"subject":[],"published":{"date-parts":[[1995,2]]}}}