{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,6]],"date-time":"2026-11-06T15:44:30Z","timestamp":1793979870612,"version":"4.8.0"},"reference-count":42,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[2004,8,13]],"date-time":"2004-08-13T00:00:00Z","timestamp":1092355200000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["BMC Med Genet"],"published-print":{"date-parts":[[2004,12]]},"DOI":"10.1186\/1471-2350-5-21","type":"journal-article","created":{"date-parts":[[2004,8,18]],"date-time":"2004-08-18T06:23:03Z","timestamp":1092810183000},"source":"Crossref","is-referenced-by-count":37,"title":["A 4q35.2 subtelomeric deletion identified in a screen of patients with co-morbid psychiatric illness and mental retardation"],"prefix":"10.1186","volume":"5","author":[{"given":"Ben S","family":"Pickard","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Edward J","family":"Hollox","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M Pat","family":"Malloy","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David J","family":"Porteous","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Douglas HR","family":"Blackwood","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"John AL","family":"Armour","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Walter J","family":"Muir","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2004,8,13]]},"reference":[{"issue":"6","key":"56_CR1","doi-asserted-by":"publisher","first-page":"401","DOI":"10.1136\/jmg.37.6.401","volume":"37","author":"SJ Knight","year":"2000","unstructured":"Knight SJ, Flint J: Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis. J Med Genet. 2000, 37 (6): 401-409. 10.1136\/jmg.37.6.401.","journal-title":"J Med Genet"},{"issue":"3","key":"56_CR2","doi-asserted-by":"crossref","first-page":"241","DOI":"10.1038\/ng917","volume":"31","author":"A Kong","year":"2002","unstructured":"Kong A, Gudbjartsson DF, Sainz J, Jonsdottir GM, Gudjonsson SA, Richardsson B, Sigurdardottir S, Barnard J, Hallbeck B, Masson G, Shlien A, Palsson ST, Frigge ML, Thorgeirsson TE, Gulcher JR, Stefansson K: A high-resolution recombination map of the human genome. Nat Genet. 2002, 31 (3): 241-247.","journal-title":"Nat Genet"},{"issue":"8","key":"56_CR3","doi-asserted-by":"publisher","first-page":"546","DOI":"10.1136\/jmg.39.8.546","volume":"39","author":"CD van Karnebeek","year":"2002","unstructured":"van Karnebeek CD, Koevoets C, Sluijter S, Bijlsma EK, Smeets DF, Redeker EJ, Hennekam RC, Hoovers JM: Prospective screening for subtelomeric rearrangements in children with mental retardation of unknown aetiology: the Amsterdam experience. J Med Genet. 2002, 39 (8): 546-553. 10.1136\/jmg.39.8.546.","journal-title":"J Med Genet"},{"key":"56_CR4","doi-asserted-by":"publisher","first-page":"1676","DOI":"10.1016\/S0140-6736(99)03070-6","volume":"354","author":"SJ Knight","year":"1999","unstructured":"Knight SJ, Regan R, Nicod A, Horsley SW, Kearney L, Homfray T, Winter RM, Bolton P, Flint J: Subtle chromosomal rearrangements in children with unexplained mental retardation. Lancet. 1999, 354: 1676-1681. 10.1016\/S0140-6736(99)03070-6.","journal-title":"Lancet"},{"issue":"7","key":"56_CR5","doi-asserted-by":"publisher","first-page":"527","DOI":"10.1038\/sj.ejhg.5200670","volume":"9","author":"C Sismani","year":"2001","unstructured":"Sismani C, Armour JA, Flint J, Girgalli C, Regan R, Patsalis PC: Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assay. Eur J Hum Genet. 2001, 9 (7): 527-532. 10.1038\/sj.ejhg.5200670.","journal-title":"Eur J Hum Genet"},{"issue":"4","key":"56_CR6","doi-asserted-by":"publisher","first-page":"285","DOI":"10.1002\/ajmg.10159","volume":"107","author":"E Baker","year":"2002","unstructured":"Baker E, Hinton L, Callen DF, Altree M, Dobbie A, Eyre HJ, Sutherland GR, Thompson E, Thompson P, Woollatt E, Haan E: Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies. Am J Med Genet. 2002, 107 (4): 285-293. 10.1002\/ajmg.10159.","journal-title":"Am J Med Genet"},{"issue":"4","key":"56_CR7","doi-asserted-by":"publisher","first-page":"440","DOI":"10.1007\/s004390100588","volume":"109","author":"CA Joyce","year":"2001","unstructured":"Joyce CA, Dennis NR, Cooper S, Browne CE: Subtelomeric rearrangements: results from a study of selected and unselected probands with idiopathic mental retardation and control individuals by using high-resolution G-banding and FISH. Hum Genet. 2001, 109 (4): 440-451. 10.1007\/s004390100588.","journal-title":"Hum Genet"},{"key":"56_CR8","first-page":"A169","volume":"59","author":"A Lamb","year":"1995","unstructured":"Lamb A, Lytle C, Aylsworth A, Powell C, Rao K, Hendrickson M, Carey J, Opitz J, Viskochil D, Leonard C, Brothman A, Stephan M, Bartley J, Hackbarth M, McCarthy D, Proffit J: Low proportion of subtelomeric rearrangements in a population of patients with mental retardation dysmorphic features. Am J Hum Genet Suppl. 1995, 59: A169-","journal-title":"Am J Hum Genet Suppl"},{"issue":"6","key":"56_CR9","first-page":"72","volume":"34","author":"SG Vorsanova","year":"2000","unstructured":"Vorsanova SG, Yurov YB, Kolotii AD, Demidova IA, Novikova IM: 16q subtelomeric deletion in proband with congenital malformations and mental retardation. Tsitol Genet. 2000, 34 (6): 72-74.","journal-title":"Tsitol Genet"},{"issue":"6","key":"56_CR10","doi-asserted-by":"publisher","first-page":"416","DOI":"10.1097\/00125817-200111000-00007","volume":"3","author":"YS Fan","year":"2001","unstructured":"Fan YS, Zhang Y, Speevak M, Farrell S, Jung JH, Siu VM: Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes. Genet Med. 2001, 3 (6): 416-421. 10.1097\/00125817-200111000-00007.","journal-title":"Genet Med"},{"issue":"3","key":"56_CR11","doi-asserted-by":"publisher","first-page":"286","DOI":"10.1007\/s004390100585","volume":"109","author":"M Riegel","year":"2001","unstructured":"Riegel M, Baumer A, Jamar M, Delbecque K, Herens C, Verloes A, Schinzel A: Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes. Hum Genet. 2001, 109 (3): 286-294. 10.1007\/s004390100585.","journal-title":"Hum Genet"},{"issue":"4","key":"56_CR12","doi-asserted-by":"publisher","first-page":"267","DOI":"10.1002\/ajmg.10240","volume":"107","author":"B Clarkson","year":"2002","unstructured":"Clarkson B, Pavenski K, Dupuis L, Kennedy S, Meyn S, Nezarati MM, Nie G, Weksberg R, Withers S, Quercia N, Teebi AS, Teshima I: Detecting rearrangements in children using subtelomeric FISH and SKY. Am J Med Genet. 2002, 107 (4): 267-274. 10.1002\/ajmg.10240.","journal-title":"Am J Med Genet"},{"issue":"1","key":"56_CR13","doi-asserted-by":"publisher","first-page":"28","DOI":"10.1097\/00125817-200301000-00005","volume":"5","author":"SM Jalal","year":"2003","unstructured":"Jalal SM, Harwood AR, Sekhon GS, Pham Lorentz C, Ketterling RP, Babovic-Vuksanovic D, Meyer RG, Ensenauer R, Anderson MH, Michels VV: Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patients. Genet Med. 2003, 5 (1): 28-34. 10.1097\/00125817-200301000-00005.","journal-title":"Genet Med"},{"issue":"9","key":"56_CR14","doi-asserted-by":"publisher","first-page":"53","DOI":"10.1136\/jmg.39.9.e53","volume":"39","author":"Z Helias-Rodzewicz","year":"2002","unstructured":"Helias-Rodzewicz Z, Bocian E, Stankiewicz P, Obersztyn E, Kostyk E, Jakubow-Durska K, Kutkowska-Kazmierczak A, Mazurczak T: Subtelomeric rearrangements detected by FISH in three of 33 families with idiopathic mental retardation and minor physical anomalies. J Med Genet. 2002, 39 (9): 53-10.1136\/jmg.39.9.e53.","journal-title":"J Med Genet"},{"issue":"4","key":"56_CR15","doi-asserted-by":"publisher","first-page":"275","DOI":"10.1002\/ajmg.10029","volume":"107","author":"BM Anderlid","year":"2002","unstructured":"Anderlid BM, Schoumans J, Anneren G, Sahlen S, Kyllerman M, Vujic M, Hagberg B, Blennow E, Nordenskjold M: Subtelomeric rearrangements detected in patients with idiopathic mental retardation. Am J Med Genet. 2002, 107 (4): 275-284. 10.1002\/ajmg.10029.","journal-title":"Am J Med Genet"},{"issue":"4","key":"56_CR16","doi-asserted-by":"publisher","first-page":"266","DOI":"10.1136\/jmg.39.4.266","volume":"39","author":"M Rio","year":"2002","unstructured":"Rio M, Molinari F, Heuertz S, Ozilou C, Gosset P, Raoul O, Cormier-Daire V, Amiel J, Lyonnet S, Le Merrer M, Turleau C, de Blois MC, Prieur M, Romana S, Vekemans M, Munnich A, Colleaux L: Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation. J Med Genet. 2002, 39 (4): 266-270. 10.1136\/jmg.39.4.266.","journal-title":"J Med Genet"},{"key":"56_CR17","first-page":"A10","volume":"63","author":"G Viot","year":"1998","unstructured":"Viot G, Gosset P, Fert S, Prieur M, Turleau C, Raoul O, De Blois MC, Lyonnet S, Munnich A, Vekemans M: Cryptic subtelomeric rearrangements detected by FISH in mentally retarded and dysmorphic patients. Am J Hum Genet Suppl. 1998, 63: A10-","journal-title":"Am J Hum Genet Suppl"},{"issue":"6","key":"56_CR18","doi-asserted-by":"publisher","first-page":"385","DOI":"10.1136\/jmg.40.6.385","volume":"40","author":"BB De Vries","year":"2003","unstructured":"De Vries BB, Winter R, Schinzel A, van Ravenswaaij-Arts C: Telomeres: a diagnosis at the end of the chromosomes. J Med Genet. 2003, 40 (6): 385-398. 10.1136\/jmg.40.6.385.","journal-title":"J Med Genet"},{"issue":"2","key":"56_CR19","doi-asserted-by":"publisher","first-page":"132","DOI":"10.1038\/ng0295-132","volume":"9","author":"J Flint","year":"1995","unstructured":"Flint J, Wilkie AO, Buckle VJ, Winter RM, Holland AJ, McDermid HE: The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation. Nat Genet. 1995, 9 (2): 132-140.","journal-title":"Nat Genet"},{"issue":"1","key":"56_CR20","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1159\/000484724","volume":"5","author":"SJ Knight","year":"1997","unstructured":"Knight SJ, Horsley SW, Regan R, Lawrie NM, Maher EJ, Cardy DL, Flint J, Kearney L: Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres. Eur J Hum Genet. 1997, 5 (1): 1-8.","journal-title":"Eur J Hum Genet"},{"issue":"2","key":"56_CR21","doi-asserted-by":"publisher","first-page":"605","DOI":"10.1093\/nar\/28.2.605","volume":"28","author":"JA Armour","year":"2000","unstructured":"Armour JA, Sismani C, Patsalis PC, Cross G: Measurement of locus copy number by hybridisation with amplifiable probes. Nucleic Acids Res. 2000, 28 (2): 605-609. 10.1093\/nar\/28.2.605.","journal-title":"Nucleic Acids Res"},{"issue":"11","key":"56_CR22","doi-asserted-by":"publisher","first-page":"790","DOI":"10.1136\/jmg.39.11.790","volume":"39","author":"EJ Hollox","year":"2002","unstructured":"Hollox EJ, Atia T, Cross G, Parkin T, Armour JA: High throughput screening of human subtelomeric DNA for copy number changes using multiplex amplifiable probe hybridisation (MAPH). J Med Genet. 2002, 39 (11): 790-795. 10.1136\/jmg.39.11.790.","journal-title":"J Med Genet"},{"issue":"4","key":"56_CR23","doi-asserted-by":"publisher","first-page":"370","DOI":"10.1586\/14737159.2.4.370","volume":"2","author":"EJ Hollox","year":"2002","unstructured":"Hollox EJ, Akrami SM, Armour JA: DNA copy number analysis by MAPH: molecular diagnostic applications. Expert Rev Mol Diagn. 2002, 2 (4): 370-378.","journal-title":"Expert Rev Mol Diagn"},{"key":"56_CR24","doi-asserted-by":"publisher","first-page":"249","DOI":"10.1136\/jmg.2003.014308","volume":"41","author":"M Kriek","year":"2004","unstructured":"Kriek M, White SJ, Bouma MC, Dauwerse HG, Hansson KB, Nijhuis JV, Bakker B, van Ommen GJ, den Dunnen JT, Breuning MH: Genomic imbalances in mental retardation. J Med Genet. 2004, 41: 249-255. 10.1136\/jmg.2003.014308.","journal-title":"J Med Genet"},{"issue":"6","key":"56_CR25","doi-asserted-by":"publisher","first-page":"531","DOI":"10.1016\/S0006-3223(00)00883-0","volume":"48","author":"WH Berrettini","year":"2000","unstructured":"Berrettini WH: Are schizophrenic and bipolar disorders related? A review of family and molecular studies. Biol Psychiatry. 2000, 48 (6): 531-538. 10.1016\/S0006-3223(00)00883-0.","journal-title":"Biol Psychiatry"},{"issue":"9","key":"56_CR26","doi-asserted-by":"publisher","first-page":"1415","DOI":"10.1093\/hmg\/9.9.1415","volume":"9","author":"JK Millar","year":"2000","unstructured":"Millar JK, Wilson-Annan JC, Anderson S, Christie S, Taylor MS, Semple CA, Devon RS, StClair DM, Muir WJ, Blackwood DH, Porteous DJ: Disruption of two novel genes by a translocation co-segregating with schizophrenia. Hum Mol Genet. 2000, 9 (9): 1415-1423. 10.1093\/hmg\/9.9.1415.","journal-title":"Hum Mol Genet"},{"issue":"1","key":"56_CR27","doi-asserted-by":"publisher","first-page":"43","DOI":"10.1007\/s10048-001-0129-x","volume":"4","author":"BE Baysal","year":"2002","unstructured":"Baysal BE, Willett-Brozick JE, Badner JA, Corona W, Ferrell RE, Nimgaonkar VL, Detera-Wadleigh SD: A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family. Neurogenetics. 2002, 4 (1): 43-53. 10.1007\/s10048-001-0129-x.","journal-title":"Neurogenetics"},{"issue":"3","key":"56_CR28","doi-asserted-by":"publisher","first-page":"356","DOI":"10.1006\/geno.1999.6032","volume":"62","author":"J Gecz","year":"1999","unstructured":"Gecz J, Barnett S, Liu J, Hollway G, Donnelly A, Eyre H, Eshkevari HS, Baltazar R, Grunn A, Nagaraja R, Gilliam C, Peltonen L, Sutherland GR, Baron M, Mulley JC: Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation. Genomics. 1999, 62 (3): 356-368. 10.1006\/geno.1999.6032.","journal-title":"Genomics"},{"key":"56_CR29","doi-asserted-by":"publisher","first-page":"145","DOI":"10.1192\/bjp.173.2.145","volume":"173","author":"GA Doody","year":"1998","unstructured":"Doody GA, Johnstone EC, Sanderson TL, Owens DG, Muir WJ: 'Pfropfschizophrenie' revisited. Schizophrenia in people with mild learning disability. Br J Psychiatry. 1998, 173: 145-153.","journal-title":"Br J Psychiatry"},{"key":"56_CR30","doi-asserted-by":"publisher","first-page":"1867","DOI":"10.1016\/S0140-6736(99)01049-1","volume":"354","author":"TL Sanderson","year":"1999","unstructured":"Sanderson TL, Best JJ, Doody GA, Owens DG, Johnstone EC: Neuroanatomy of comorbid schizophrenia and learning disability: a controlled study. Lancet. 1999, 354: 1867-1871. 10.1016\/S0140-6736(99)01049-1.","journal-title":"Lancet"},{"key":"56_CR31","doi-asserted-by":"publisher","first-page":"837","DOI":"10.1001\/archpsyc.1978.01770310043002","volume":"35","author":"J Endicott","year":"1978","unstructured":"Endicott J, Spitzer RL: A diagnostic interview: the schedule for affective disorders and schizophrenia. Arch Gen Psychiatry. 1978, 35: 837-844.","journal-title":"Arch Gen Psychiatry"},{"key":"56_CR32","volume-title":"Diagnostic and Statistical Manual of Mental Disorders. Text Revision","author":"American Psychiatric Association","year":"2000","unstructured":"American Psychiatric Association: Diagnostic and Statistical Manual of Mental Disorders. Text Revision. 2000, American Psychiatric Association, Washington, DC, 4","edition":"4"},{"key":"56_CR33","doi-asserted-by":"publisher","first-page":"1077","DOI":"10.1086\/340363","volume":"70","author":"HE McDermid","year":"2002","unstructured":"McDermid HE, Morrow BE: Genomic disorders on 22q11. Am J Hum Genet. 2002, 70: 1077-1088. 10.1086\/340363.","journal-title":"Am J Hum Genet"},{"key":"56_CR34","doi-asserted-by":"publisher","first-page":"397","DOI":"10.1192\/bjp.179.5.397","volume":"179","author":"KC Murphy","year":"2001","unstructured":"Murphy KC, Owen MJ: Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia. Br J Psychiatry. 2001, 179: 397-402. 10.1192\/bjp.179.5.397.","journal-title":"Br J Psychiatry"},{"key":"56_CR35","doi-asserted-by":"publisher","first-page":"858","DOI":"10.1038\/35098574","volume":"2","author":"EA Lindsay","year":"2001","unstructured":"Lindsay EA: Chromosomal microdeletions: dissecting del22q11 syndrome. Nat Rev Genet. 2001, 2: 858-868. 10.1038\/35098574.","journal-title":"Nat Rev Genet"},{"issue":"5","key":"56_CR36","doi-asserted-by":"publisher","first-page":"1084","DOI":"10.1086\/301826","volume":"62","author":"LJ Adams","year":"1998","unstructured":"Adams LJ, Mitchell PB, Fielder SL, Rosso A, Donald JA, Schofield PR: A susceptibility locus for bipolar affective disorder on chromosome 4q35. Am J Hum Genet. 1998, 62 (5): 1084-1091. 10.1086\/301826.","journal-title":"Am J Hum Genet"},{"issue":"8","key":"56_CR37","doi-asserted-by":"publisher","first-page":"867","DOI":"10.1038\/sj.mp.4001113","volume":"7","author":"IP Blair","year":"2002","unstructured":"Blair IP, Adams LJ, Badenhop RF, Moses MJ, Scimone A, Morris JA, Ma L, Austin CP, Donald JA, Mitchell PB, Schofield PR: A transcript map encompassing a susceptibility locus for bipolar affective disorder on chromosome 4q35. Mol Psychiatry. 2002, 7 (8): 867-873. 10.1038\/sj.mp.4001113.","journal-title":"Mol Psychiatry"},{"issue":"1","key":"56_CR38","doi-asserted-by":"publisher","first-page":"23","DOI":"10.1002\/ajmg.b.10023","volume":"117B","author":"RF Badenhop","year":"2003","unstructured":"Badenhop RF, Moses MJ, Scimone A, Adams LJ, Kwok JB, Jones AM, Davison G, Evans MR, Kirkby KC, Hewitt JE, Donald JA, Mitchell PB, Schofield PR: Genetic refinement and physical mapping of a 2.3 Mb probable disease region associated with a bipolar affective disorder susceptibility locus on chromosome 4q35. Am J Med Genet. 2003, 117B (1): 23-32. 10.1002\/ajmg.b.10023.","journal-title":"Am J Med Genet"},{"issue":"4","key":"56_CR39","doi-asserted-by":"publisher","first-page":"332","DOI":"10.1007\/s11920-001-0030-1","volume":"3","author":"E Bramon","year":"2001","unstructured":"Bramon E, Sham PC: The common genetic liability between schizophrenia and bipolar disorder: a review. Curr Psychiatry Rep. 2001, 3 (4): 332-337.","journal-title":"Curr Psychiatry Rep"},{"issue":"5","key":"56_CR40","doi-asserted-by":"publisher","first-page":"366","DOI":"10.1136\/jmg.33.5.366","volume":"33","author":"R Tupler","year":"1996","unstructured":"Tupler R, Berardinelli A, Barbierato L, Frants R, Hewitt JE, Lanzi G, Maraschio P, Tiepolo L: Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy. J Med Genet. 1996, 33 (5): 366-370.","journal-title":"J Med Genet"},{"issue":"2","key":"56_CR41","doi-asserted-by":"publisher","first-page":"235","DOI":"10.1038\/ng999","volume":"32","author":"RJ Lemmers","year":"2002","unstructured":"Lemmers RJ, de Kievit P, Sandkuijl L, Padberg GW, van Ommen GJ, Frants RR, van der Maarel SM: Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere. Nat Genet. 2002, 32 (2): 235-236. 10.1038\/ng999.","journal-title":"Nat Genet"},{"issue":"3","key":"56_CR42","doi-asserted-by":"publisher","first-page":"175","DOI":"10.1136\/jmg.38.3.175","volume":"38","author":"BB De Vries","year":"2001","unstructured":"De Vries BB, Knight SJ, Homfray T, Smithson SF, Flint J, Winter RM: Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype?. J Med Genet. 2001, 38 (3): 175-178. 10.1136\/jmg.38.3.175.","journal-title":"J Med Genet"}],"container-title":["BMC Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1186\/1471-2350-5-21.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1186\/1471-2350-5-21\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1186\/1471-2350-5-21","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,4,3]],"date-time":"2020-04-03T00:25:30Z","timestamp":1585873530000},"score":1,"resource":{"primary":{"URL":"http:\/\/bmcmedgenet.biomedcentral.com\/articles\/10.1186\/1471-2350-5-21"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2004,8,13]]},"references-count":42,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2004,12]]}},"alternative-id":["56"],"URL":"https:\/\/doi.org\/10.1186\/1471-2350-5-21","relation":{},"ISSN":["1471-2350"],"issn-type":[{"value":"1471-2350","type":"electronic"}],"subject":[],"published":{"date-parts":[[2004,8,13]]},"article-number":"21"}}