{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,8,5]],"date-time":"2024-08-05T21:30:38Z","timestamp":1722893438362},"reference-count":25,"publisher":"Springer Science and Business Media LLC","issue":"12","license":[{"start":{"date-parts":[[2008,5,27]],"date-time":"2008-05-27T00:00:00Z","timestamp":1211846400000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Br J Cancer"],"published-print":{"date-parts":[[2008,6]]},"DOI":"10.1038\/sj.bjc.6604391","type":"journal-article","created":{"date-parts":[[2008,5,27]],"date-time":"2008-05-27T14:22:01Z","timestamp":1211898121000},"page":"1929-1933","source":"Crossref","is-referenced-by-count":10,"title":["Cancer risk in patients with constitutional chromosome deletions: a nationwide British cohort study"],"prefix":"10.1038","volume":"98","author":[{"name":"on behalf of the UK Clinical Cytogenetics Group","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A J","family":"Swerdlow","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M J","family":"Schoemaker","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C D","family":"Higgins","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A F","family":"Wright","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P A","family":"Jacobs","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2008,5,27]]},"reference":[{"key":"BF6604391_CR1","volume-title":"Practical Statistics for Medical Research","author":"DG Altman","year":"1991","unstructured":"Altman DG (1991) Practical Statistics for Medical Research. Boca Raton: Chapman & Hall\/CRC"},{"key":"BF6604391_CR2","doi-asserted-by":"publisher","first-page":"231","DOI":"10.1002\/gcc.20285","volume":"45","author":"I Bache","year":"2006","unstructured":"Bache I, Hasle H, Tommerup N, Olsen JH (2006) Population-based study of cancer among carriers of a constitutional structural chromosomal rearrangement. Genes Chromosomes Cancer 45: 231\u2013246","journal-title":"Genes Chromosomes Cancer"},{"key":"BF6604391_CR3","doi-asserted-by":"publisher","first-page":"345","DOI":"10.1016\/0165-4608(87)90117-8","volume":"24","author":"J Benitez","year":"1987","unstructured":"Benitez J, Valcarcel E, Ramos C, Ayuso C, Cascos AS (1987) Frequency of constitutional chromosome alterations in patients with hematologic neoplasias. Cancer Genet Cytogenet 24: 345\u2013354","journal-title":"Cancer Genet Cytogenet"},{"key":"BF6604391_CR4","volume-title":"Statistical Methods in Cancer Research. Volume II \u2013 The Design and Analysis of Cohort Studies","author":"NE Breslow","year":"1987","unstructured":"Breslow NE, Day NE (1987) Statistical Methods in Cancer Research. Volume II \u2013 The Design and Analysis of Cohort Studies. IARC Scientific Publication No. 82. International Agency for Research on Cancer: Lyon"},{"key":"BF6604391_CR5","doi-asserted-by":"publisher","first-page":"133","DOI":"10.1016\/S0165-4608(01)00621-5","volume":"134","author":"R Cerretini","year":"2002","unstructured":"Cerretini R, Acevedo S, Chena C, Belli C, Larripa I, Slavutsky I (2002) Evaluation of constitutional chromosome aberrations in hematologic disorders. Cancer Genet Cytogenet 134: 133\u2013137","journal-title":"Cancer Genet Cytogenet"},{"key":"BF6604391_CR6","doi-asserted-by":"publisher","first-page":"398","DOI":"10.1016\/S0022-3476(98)70008-3","volume":"132","author":"MR DeBaun","year":"1998","unstructured":"DeBaun MR, Tucker MA (1998) Risk of cancer during the first four years of life in children from The Beckwith\u2013Wiedemann Syndrome Registry. J Pediatr 132: 398\u2013400","journal-title":"J Pediatr"},{"key":"BF6604391_CR7","doi-asserted-by":"publisher","first-page":"320","DOI":"10.1002\/jcb.21481","volume":"102","author":"P Gasparini","year":"2007","unstructured":"Gasparini P, Sozzi G, Pierotti MA (2007) The role of chromosomal alterations in human cancer development. J Cell Biochem 102: 320\u2013331","journal-title":"J Cell Biochem"},{"key":"BF6604391_CR8","doi-asserted-by":"publisher","first-page":"51","DOI":"10.1002\/ajmg.a.30090","volume":"129A","author":"PD Grossfeld","year":"2004","unstructured":"Grossfeld PD, Mattina T, Lai Z, Favier R, Jones KL, Cotter F, Jones C (2004) The 11q terminal deletion disorder: a prospective study of 110 cases. Am J Med Genet 129A: 51\u201361","journal-title":"Am J Med Genet"},{"key":"BF6604391_CR9","doi-asserted-by":"publisher","first-page":"223","DOI":"10.1111\/j.1399-0004.1975.tb01498.x","volume":"8","author":"JL Hamerton","year":"1975","unstructured":"Hamerton JL, Canning N, Ray M, Smith S (1975) A cytogenetic survey of 14\u2009069 newborn infants. I. Incidence of chromosome abnormalities. Clin Genet 8: 223\u2013243","journal-title":"Clin Genet"},{"key":"BF6604391_CR10","doi-asserted-by":"publisher","first-page":"6953","DOI":"10.1073\/pnas.91.15.6953","volume":"91","author":"GM Hampton","year":"1994","unstructured":"Hampton GM, Penny LA, Baergen RN, Larson A, Brewer C, Liao S, Busby-Earle RMC, Williams AWR, Steel CM, Bird CM, Stanbridge EJ, Evans GA (1994) Loss of heterozygosity in cervical carcinoma: subchromosomal localization of a putative tumor-suppressor gene to chromosome 11q22\u2013q24. Proc Natl Acad Sci USA 91: 6953\u20136957","journal-title":"Proc Natl Acad Sci USA"},{"key":"BF6604391_CR11","doi-asserted-by":"publisher","first-page":"103","DOI":"10.1136\/jmg.29.2.103","volume":"29","author":"PA Jacobs","year":"1992","unstructured":"Jacobs PA, Browne C, Gregson N, Joyce C, White H (1992) Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding. J Med Genet 29: 103\u2013108","journal-title":"J Med Genet"},{"key":"BF6604391_CR12","doi-asserted-by":"publisher","first-page":"2123","DOI":"10.1093\/hmg\/3.12.2123","volume":"3","author":"C Jones","year":"1994","unstructured":"Jones C, Slijepcevic P, Marsh S, Baker E, Langdon WY, Richards RI, Tunnacliffe A (1994) Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3. Hum Mol Genet 3: 2123\u20132130","journal-title":"Hum Mol Genet"},{"key":"BF6604391_CR13","doi-asserted-by":"publisher","first-page":"137","DOI":"10.1002\/gcc.10263","volume":"38","author":"F Micci","year":"2003","unstructured":"Micci F, Teixeira MR, Scheistroen M, Abeler VM, Heim S (2003) Cytogenetic characterization of tumors of the vulva and vagina. Genes Chromosomes Cancer 38: 137\u2013148","journal-title":"Genes Chromosomes Cancer"},{"key":"BF6604391_CR14","doi-asserted-by":"publisher","first-page":"417","DOI":"10.1038\/ng0497supp-417","volume":"15","author":"F Mitelman","year":"1997","unstructured":"Mitelman F, Mertens F, Johansson B (1997) A breakpoint map of recurrent chromosomal rearrangements in human neoplasia. Nat Genet 15: 417\u2013474","journal-title":"Nat Genet"},{"key":"BF6604391_CR15","doi-asserted-by":"publisher","first-page":"595","DOI":"10.1002\/ijc.2910390509","volume":"39","author":"M Muleris","year":"1987","unstructured":"Muleris M, Salmon RJ, Girodet J, Zafrani B, Dutrillaux B (1987) Recurrent deletions of chromosomes 11q and 3p in anal canal carcinoma. Int J Cancer 39: 595\u2013598","journal-title":"Int J Cancer"},{"key":"BF6604391_CR16","doi-asserted-by":"publisher","first-page":"475","DOI":"10.1053\/hupa.2001.24317","volume":"32","author":"MJ O\u2032Sullivan","year":"2001","unstructured":"O\u2032Sullivan MJ, Rader JS, Gerhard DS, Li Y, Trinkaus KM (2001) Loss of heterozygosity at 11q23.3 in vasculoinvasive and metastatic squamous cell carcinoma of the cervix. Hum Pathol 32: 475\u2013478","journal-title":"Hum Pathol"},{"key":"BF6604391_CR17","doi-asserted-by":"publisher","first-page":"1009","DOI":"10.1016\/S0002-9440(10)65353-9","volume":"154","author":"AP Pinto","year":"1999","unstructured":"Pinto AP, Lin MC, Mutter GL, Sun D, Villa LL, Crum CP (1999) Allelic loss in human papillomavirus-positive and -negative vulvar squamous cell carcinomas. Am J Pathol 154: 1009\u20131015","journal-title":"Am J Pathol"},{"key":"BF6604391_CR18","first-page":"6677","volume":"60","author":"HA Pulido","year":"2000","unstructured":"Pulido HA, Fakruddin MJ, Chatterjee A, Esplin ED, Beleno N, Martinez G, Posso H, Evans GA, Murty VV (2000) Identification of a 6-cM minimal deletion at 11q23.1\u201323.2 and exclusion of PPP2R1B gene as a deletion target in cervical cancer. Cancer Res 60: 6677\u20136682","journal-title":"Cancer Res"},{"key":"BF6604391_CR19","doi-asserted-by":"publisher","first-page":"659","DOI":"10.1016\/S0959-8049(98)00413-4","volume":"35","author":"H Skomedal","year":"1999","unstructured":"Skomedal H, Helland A, Kristensen GB, Holm R, Borresen-Dale AL (1999) Allelic imbalance at chromosome region 11q23 in cervical carcinomas. Eur J Cancer 35: 659\u2013663","journal-title":"Eur J Cancer"},{"key":"BF6604391_CR20","doi-asserted-by":"crossref","unstructured":"Smith DI, Zhu Y, McAvoy S, Kuhn R (2006) Common fragile sites, extremely large genes, neural development and cancer. Cancer Letters 232: 48\u201357","DOI":"10.1016\/j.canlet.2005.06.049"},{"key":"BF6604391_CR21","doi-asserted-by":"publisher","DOI":"10.1093\/acprof:oso\/9780192627483.001.0001","volume-title":"Cancer Incidence and Mortality in England and Wales: Trends and Risk Factors","author":"A Swerdlow","year":"2001","unstructured":"Swerdlow A, dos Santos Silva I, Doll R (2001) Cancer Incidence and Mortality in England and Wales: Trends and Risk Factors. Oxford: Oxford University Press"},{"key":"BF6604391_CR22","unstructured":"UCSC Genome Browser (2006) \n                    http:\/\/genome.ucsc.edu\/cgi-bin\/hgTracks"},{"key":"BF6604391_CR23","doi-asserted-by":"publisher","first-page":"137","DOI":"10.1016\/S0165-4608(03)00301-7","volume":"149","author":"J Welborn","year":"2004","unstructured":"Welborn J (2004) Constitutional chromosome aberrations as pathogenetic events in hematologic malignancies. Cancer Genet Cytogenet 149: 137\u2013153","journal-title":"Cancer Genet Cytogenet"},{"key":"BF6604391_CR24","unstructured":"World Health Organization (1977) Manual of the International Statistical Classification of Diseases, Injuries, and Causes of Death, 9th revision, Vol 1. World Health Organization: Geneva"},{"key":"BF6604391_CR25","doi-asserted-by":"publisher","first-page":"227","DOI":"10.1126\/science.6336310","volume":"221","author":"JJ Yunis","year":"1983","unstructured":"Yunis JJ (1983) The chromosomal basis of human neoplasia. Science 221: 227\u2013236","journal-title":"Science"}],"container-title":["British Journal of Cancer"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/www.nature.com\/articles\/6604391.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/www.nature.com\/articles\/6604391","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/www.nature.com\/articles\/6604391.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,18]],"date-time":"2023-05-18T12:33:13Z","timestamp":1684413193000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.nature.com\/articles\/6604391"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,5,27]]},"references-count":25,"journal-issue":{"issue":"12","published-print":{"date-parts":[[2008,6]]}},"alternative-id":["BF6604391"],"URL":"https:\/\/doi.org\/10.1038\/sj.bjc.6604391","relation":{},"ISSN":["0007-0920","1532-1827"],"issn-type":[{"type":"print","value":"0007-0920"},{"type":"electronic","value":"1532-1827"}],"subject":[],"published":{"date-parts":[[2008,5,27]]}}}