{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,4]],"date-time":"2026-10-04T19:19:17Z","timestamp":1791141557042,"version":"4.1.0"},"reference-count":48,"publisher":"Springer Science and Business Media LLC","issue":"7","license":[{"start":{"date-parts":[[2008,3,19]],"date-time":"2008-03-19T00:00:00Z","timestamp":1205884800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Ann Hematol"],"published-print":{"date-parts":[[2008,7]]},"DOI":"10.1007\/s00277-008-0462-3","type":"journal-article","created":{"date-parts":[[2008,3,18]],"date-time":"2008-03-18T16:37:31Z","timestamp":1205858251000},"page":"537-544","source":"Crossref","is-referenced-by-count":32,"title":["Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regions"],"prefix":"10.1007","volume":"87","author":[{"given":"Nathalie","family":"Douet-Guilbert","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Audrey","family":"Basinko","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fr\u00e9d\u00e9ric","family":"Morel","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marie-Jos\u00e9e","family":"Le Bris","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Val\u00e9rie","family":"Ugo","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Patrick","family":"Morice","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christian","family":"Berthou","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marc","family":"De Braekeleer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2008,3,19]]},"reference":[{"key":"462_CR1","doi-asserted-by":"crossref","first-page":"507","DOI":"10.1016\/S0025-6196(12)60566-7","volume":"60","author":"RH Knapp","year":"1985","unstructured":"Knapp RH, Dewald GW, Pierre RV (1985) Cytogenetic studies in 174 consecutive patients with preleukemic or myelodysplastic syndromes. Mayo Clin Proc 60:507\u2013516","journal-title":"Mayo Clin Proc"},{"key":"462_CR2","doi-asserted-by":"crossref","first-page":"233","DOI":"10.1016\/0165-4608(87)90183-X","volume":"25","author":"G Rege-Cambrin","year":"1987","unstructured":"Rege-Cambrin G, Mecucci C, Tricot G, Michaux JL, Louwagie A, Van Hove W, Francart H, Van den Berghe H (1987) A chromosomal profile of polycythemia vera. Cancer Genet Cytogenet 25:233\u2013245","journal-title":"Cancer Genet Cytogenet"},{"key":"462_CR3","doi-asserted-by":"crossref","first-page":"819","DOI":"10.1016\/S0950-3536(98)80041-3","volume":"11","author":"AJ Bench","year":"1998","unstructured":"Bench AJ, Nacheva EP, Champion KM, Green AR (1998) Molecular genetics and cytogenetics of myeloproliferative disorders. Baillieres Clin Haematol 11:819\u2013848","journal-title":"Baillieres Clin Haematol"},{"key":"462_CR4","doi-asserted-by":"crossref","first-page":"29","DOI":"10.1002\/ajh.2830110105","volume":"11","author":"JR Testa","year":"1981","unstructured":"Testa JR, Kanofsky JR, Rowley JD, Baron JM, Vardiman JW (1981) Karyotypic patterns and their clinical significance in polycythemia vera. Am J Hematol 11:29\u201345","journal-title":"Am J Hematol"},{"key":"462_CR5","doi-asserted-by":"crossref","first-page":"855","DOI":"10.1182\/blood.V72.3.855.bloodjournal723855","volume":"72","author":"JL Demory","year":"1988","unstructured":"Demory JL, Dupriez B, Fenaux P, Lai JL, Beuscart R, Jouet JP, Deminatti M, Bauters F (1988) Cytogenetic studies and their prognostic significance in agnogenic myeloid metaplasia: a report on 47 cases. Blood 72:855\u2013859","journal-title":"Blood"},{"key":"462_CR6","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1016\/j.cancergencyto.2006.09.021","volume":"173","author":"V Djordjevic","year":"2007","unstructured":"Djordjevic V, Dencic-Fekete M, Jovanovic J, Bizic S, Jankovic G, Bogdanovic A, Cemerikic-Martinovic V, Gotic M (2007) Cytogenetics of agnogenic myeloid metaplasia: a study of 61 patients. Cancer Genet Cytogenet 173:57\u201362","journal-title":"Cancer Genet Cytogenet"},{"key":"462_CR7","doi-asserted-by":"crossref","first-page":"82","DOI":"10.1016\/0165-4608(95)00260-X","volume":"87","author":"C Brigaudeau","year":"1996","unstructured":"Brigaudeau C, Liozon E, Bernard P, Trimoreau F, Bordessoule D, Praloran V (1996) Deletion of chromosome 20q associated with hypereosinophilic syndrome. Cancer Genet Cytogenet 87:82\u201384","journal-title":"Cancer Genet Cytogenet"},{"key":"462_CR8","doi-asserted-by":"crossref","first-page":"2292","DOI":"10.1182\/blood-2002-04-1199","volume":"100","author":"JW Vardiman","year":"2002","unstructured":"Vardiman JW, Harris NL, Brunning RD (2002) The World Health Organization (WHO) classification of the myeloid neoplasms. Blood 100:2292\u20132302","journal-title":"Blood"},{"key":"462_CR9","doi-asserted-by":"crossref","first-page":"189","DOI":"10.1111\/j.1365-2141.1982.tb08475.x","volume":"51","author":"JM Bennett","year":"1982","unstructured":"Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton DA, Gralnick HR, Sultan C (1982) Proposals for the classification of the myelodysplastic syndromes. Br J Haematol 51:189\u2013199","journal-title":"Br J Haematol"},{"key":"462_CR10","first-page":"9","volume":"36","author":"S Murphy","year":"1999","unstructured":"Murphy S (1999) Diagnostic criteria and prognosis in polycythemia vera and essential thrombocythemia. Semin Hematol 36:9\u201313","journal-title":"Semin Hematol"},{"key":"462_CR11","doi-asserted-by":"crossref","first-page":"457","DOI":"10.1111\/j.1600-0609.2007.00847.x","volume":"78","author":"A Herry","year":"2007","unstructured":"Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, De Braekeleer M (2007) Redefining monosomy 5 by molecular cytogenetics in 23 patients with MDS\/AML. Eur J Haematol 78:457\u2013467","journal-title":"Eur J Haematol"},{"key":"462_CR12","unstructured":"ISCN (2005) An international system for human cytogenetic nomenclature. Karger, Basel"},{"key":"462_CR13","doi-asserted-by":"crossref","first-page":"160","DOI":"10.1002\/ajmg.a.30939","volume":"138","author":"L Pinson","year":"2005","unstructured":"Pinson L, Perrin A, Plouzennec C, Parent P, Metz C, Collet M, Le Bris MJ, Douet-Guilbert N, Morel F, De Braekeleer M (2005) Detection of an unexpected subtelomeric 15q26.2\u2192qter deletion in a litte girl: clinical and cytogenetic studies. Am J Med Genet 138:160\u2013165","journal-title":"Am J Med Genet"},{"key":"462_CR14","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1016\/0165-4608(84)90009-8","volume":"12","author":"MP Davis","year":"1984","unstructured":"Davis MP, Dewald GW, Pierre RV, Hoagland HC (1984) Hematologic manifestations associated with deletions of the long arm of chromosome 20. Cancer Genet Cytogenet 12:63\u201371","journal-title":"Cancer Genet Cytogenet"},{"key":"462_CR15","doi-asserted-by":"crossref","first-page":"6692","DOI":"10.1073\/pnas.82.19.6692","volume":"82","author":"MM Beau Le","year":"1985","unstructured":"Le Beau MM, Westbrook CA, Diaz MO, Rowley JD (1985) c-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disorders. Proc Natl Acad Sci USA 82:6692\u20136696","journal-title":"Proc Natl Acad Sci USA"},{"key":"462_CR16","first-page":"3424","volume":"82","author":"D Roulston","year":"1993","unstructured":"Roulston D, Espinosa RI, Stoffel M, Bell GI, Le Beau MM (1993) Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20. Blood 82:3424\u20133429","journal-title":"Blood"},{"key":"462_CR17","doi-asserted-by":"crossref","first-page":"3086","DOI":"10.1182\/blood.V84.9.3086.3086","volume":"84","author":"FA Asimakopoulos","year":"1994","unstructured":"Asimakopoulos FA, White NJ, Nacheva E, Green AR (1994) Molecular analysis of chromosome 20q deletions associated with myeloproliferative disorders and myelodysplastic syndromes. Blood 84:3086\u20133094","journal-title":"Blood"},{"key":"462_CR18","doi-asserted-by":"crossref","first-page":"351","DOI":"10.1006\/geno.1998.5231","volume":"49","author":"AJ Bench","year":"1998","unstructured":"Bench AJ, Aldred MA, Humphray SJ, Champion KM, Gilbert JGR, Asimakopoulos FA, Deloukas P, Gwilliam R, Bentley DR, Green AR (1998) A detailed physical and transcriptional map of the region of chromosome 20 that is deleted in myeloproliferative disorders and refinement of the commonly deleted segment. Genomics 49:351\u2013362","journal-title":"Genomics"},{"key":"462_CR19","doi-asserted-by":"crossref","first-page":"3902","DOI":"10.1038\/sj.onc.1203728","volume":"19","author":"AJ Bench","year":"2000","unstructured":"Bench AJ, Nacheva EP, Hood TL, Holden JL, French L, Swanton S, Champion KM, Li J, Whittaker P, Stavrides G, Hunt AR, Huntly BJP, Campbell LJ, Bentley DR, Deloukas P, Green AR (2000) Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC\/BAC contig and identification of candidate genes. UK Cancer Cytogenetics Group (UKCCG) Oncogene 19:3902\u20133913","journal-title":"Oncogene"},{"key":"462_CR20","doi-asserted-by":"crossref","first-page":"28","DOI":"10.1006\/geno.2000.6215","volume":"68","author":"PW Wang","year":"2000","unstructured":"Wang PW, Eisenbart JD, Espinosa RI, Davis EM, Larson RA, Le Beau MM (2000) Refinement of the smallest commonly deleted segment of chromosome 20 in malignant myeloid diseases and development of a PAC-based physical and transcription map. Genomics 68:28\u201332","journal-title":"Genomics"},{"key":"462_CR21","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1002\/(SICI)1098-2264(199802)21:2<75::AID-GCC1>3.0.CO;2-4","volume":"21","author":"PW Wang","year":"1998","unstructured":"Wang PW, Iannantuoni K, Davis EM, Espinosa R III, Stoffel M, Le Beau MM (1998) Refinement of the commonly deleted segment in myeloid leukemias with a del(20q). Genes, Chromosomes & Cancer 21:75\u201381","journal-title":"Genes, Chromosomes & Cancer"},{"key":"462_CR22","doi-asserted-by":"crossref","first-page":"4150","DOI":"10.1038\/sj.onc.1204540","volume":"20","author":"D MacGrogan","year":"2001","unstructured":"MacGrogan D, Alvarez S, DeBlasio T, Jhanwar S, Nimer SD (2001) Identification of candidate genes on chromosome band 20q12 by physical mapping of translocation breakpoints found in myeloid leukemia cell lines. Oncogene 20:4150\u20134160","journal-title":"Oncogene"},{"key":"462_CR23","doi-asserted-by":"crossref","first-page":"3799","DOI":"10.1038\/sj.onc.1202732","volume":"18","author":"H Koga","year":"1999","unstructured":"Koga H, Matsui S, Hirota T, Takebayashi S, Okumura K, Saya H (1999) A human homolog of Drosophila lethal(3)malignant brain tumor (l(3)mbt) protein associates with condensed mitotic chromosomes. Oncogene 18:3799\u20133809","journal-title":"Oncogene"},{"key":"462_CR24","doi-asserted-by":"crossref","first-page":"7341","DOI":"10.1073\/pnas.0308195101","volume":"101","author":"J Li","year":"2004","unstructured":"Li J, Bench AJ, Vassiliou GS, Fourouclas N, Ferguson-Smith AC, Green AR (2004) Imprinting of the human L3MBTL gene, a polycomb family mamver located in region of chromosome 20 deleted in human myeloid malignancies. Proc Natl Acad Sci USA 101:7341\u20137346","journal-title":"Proc Natl Acad Sci USA"},{"key":"462_CR25","doi-asserted-by":"crossref","first-page":"203","DOI":"10.1002\/gcc.20087","volume":"4","author":"D MacGrogan","year":"2004","unstructured":"MacGrogan D, Kalakonda N, Alvarez S, Scandura JM, Boccuni P, Johansson B, Nimer SD (2004) Structural integrity and expression of the L3MBTL gene in normal and malignant hematopoietic cells. Genes, Chromosomes & Cancer 4:203\u2013213","journal-title":"Genes, Chromosomes & Cancer"},{"key":"462_CR26","doi-asserted-by":"crossref","first-page":"1121","DOI":"10.1158\/1078-0432.CCR-05-1766","volume":"12","author":"Y Ma","year":"2006","unstructured":"Ma Y, Lin D, Sun W, Xiao T, Yuan J, Han N, Guo S, Feng X, Su K, Mao Y, Cheng S, Gao Y (2006) Expression of targeting protein for Xklp2 associated with both malignant transformation of respiratory epithelium and progression of squamous cell lung cancer. Clin Cancer Res 12:1121\u20131127","journal-title":"Clin Cancer Res"},{"key":"462_CR27","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1002\/gcc.20385","volume":"46","author":"RN Mackinnon","year":"2007","unstructured":"Mackinnon RN, Patsouris C, Chudoba I, Campbell LJ (2007) A FISH comparison of variant derivatives of the recurrent dic(17;20) of myelodysplastic syndromes and acute myeloid leukemia: obligatory retention of genes on 17p and 20q may explain the formation of dicentric chromosomes. Genes, Chromosomes & Cancer 46:27\u201336","journal-title":"Genes, Chromosomes & Cancer"},{"key":"462_CR28","doi-asserted-by":"crossref","first-page":"699","DOI":"10.1038\/25387","volume":"396","author":"RM Pitti","year":"1998","unstructured":"Pitti RM, Marsters SA, Lawrence DA, Roy M, Kischkel FC, Dowd P, Huang A, Donahue CJ, Sherwood SW, Baldwin DT, Godowski PJ, Wood WI, Gurney AL, Hillan KJ, Cohen RL, Goddard AD, Botstein D, Ashkenazi A (1998) Genomic amplification of a decoy receptor for Fas ligand in lung and colon cancer. Nature 396:699\u2013703","journal-title":"Nature"},{"key":"462_CR29","doi-asserted-by":"crossref","first-page":"282","DOI":"10.1309\/XK594E4B5WU82QR6","volume":"124","author":"H Li","year":"2005","unstructured":"Li H, Zhang L, Lou H, Ding I, Kim S, Wang L, Huang J, Di Sant'Agnese PA, Lei JY (2005) Overexpression of decoy receptor 3 in precancerous lesions and adenocarcinoma of the esophagus. Am J Clin Pathol 124:282\u2013287","journal-title":"Am J Clin Pathol"},{"key":"462_CR30","doi-asserted-by":"crossref","first-page":"3216","DOI":"10.1128\/MCB.23.9.3216-3225.2003","volume":"23","author":"D Garcia-Domingo","year":"2003","unstructured":"Garcia-Domingo D, Ramirez D, Gonzalez DB, Martinez A (2003) Death inducer-obliterator I triggers apoptosis after nuclear translocation and caspase upregulation. Mol Cell Biol 23:3216\u20133225","journal-title":"Mol Cell Biol"},{"key":"462_CR31","doi-asserted-by":"crossref","first-page":"2351","DOI":"10.1172\/JCI24177","volume":"115","author":"A Futterer","year":"2005","unstructured":"Futterer A, Campanero MR, Leonardo E, Criado LM, Flores JM, Hernandez JM, San Miguel JF, Martinez AC (2005) Dido gene expression alterations are implicated in the induction of hematological myeloid neoplasms. J Clin Invest 115:2351\u20132362","journal-title":"J Clin Invest"},{"key":"462_CR32","doi-asserted-by":"crossref","first-page":"977","DOI":"10.1016\/j.biocel.2004.10.012","volume":"37","author":"F Rodier","year":"2005","unstructured":"Rodier F, Kim SH, Nijjar T, Yaswen P, Campisi J (2005) Cancer and aging: the importance of telomeres in genome maintenance. Int J Biochem Cell Biol 37:977\u2013990","journal-title":"Int J Biochem Cell Biol"},{"key":"462_CR33","doi-asserted-by":"crossref","first-page":"1000","DOI":"10.1016\/j.biocel.2004.09.003","volume":"37","author":"D Gilley","year":"2005","unstructured":"Gilley D, Tanaka H, Herbert BS (2005) Telomere dysfunction in aging and cancer. Int J Biochem Cell Biol 37:1000\u20131013","journal-title":"Int J Biochem Cell Biol"},{"key":"462_CR34","first-page":"265","volume-title":"Telomeres","author":"T Lange De","year":"1995","unstructured":"De Lange T (1995) Telomere dynamics and genome instability in human cancer. In: Blackburn EH, Greider CW (eds) Telomeres. Cold Spring Harbor, Plainview, NY, pp 265\u2013293"},{"key":"462_CR35","doi-asserted-by":"crossref","first-page":"1164","DOI":"10.1002\/bies.20125","volume":"26","author":"JP Murnane","year":"2004","unstructured":"Murnane JP, Sabatier L (2004) Chromosome rearrangements resulting from telomere dysfunction and their role in cancer. BioEssays 26:1164\u20131174","journal-title":"BioEssays"},{"key":"462_CR36","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1158\/1541-7786.MCR-04-0194","volume":"3","author":"L Sabatier","year":"2005","unstructured":"Sabatier L, Ricoul M, Pottier G, Murnane JP (2005) The loss of a single telomere can result in instability of multiple chromosomes in a human tumor cell line. Mol Cancer Res 3:139\u2013150","journal-title":"Mol Cancer Res"},{"key":"462_CR37","first-page":"127","volume":"33","author":"P Fenaux","year":"1996","unstructured":"Fenaux P, Morel P, Lai JL (1996) Cytogenetics of myelodysplastic syndromes. Semin Hematol 33:127\u2013138","journal-title":"Semin Hematol"},{"key":"462_CR38","first-page":"258","volume":"83","author":"T Vallespi","year":"1998","unstructured":"Vallespi T, Imbert M, Mecucci C, Preudhomme C, Fenaux P (1998) Diagnosis, classification, and cytogenetics of myelodysplastic syndromes. Haematologica 83:258\u2013275","journal-title":"Haematologica"},{"key":"462_CR39","doi-asserted-by":"crossref","first-page":"9","DOI":"10.1016\/j.cancergencyto.2006.06.003","volume":"171","author":"YC Liu","year":"2006","unstructured":"Liu YC, Ito Y, Hsiao HH, Sashida G, Kodama A, Ohyashiki JH, Ohyashiki K (2006) Risk factor analysis in myelodysplastic syndrome patients with del(20q): prognosis revisited. Cancer Genet Cytogenet 171:9\u201316","journal-title":"Cancer Genet Cytogenet"},{"key":"462_CR40","doi-asserted-by":"crossref","first-page":"2079","DOI":"10.1182\/blood.V89.6.2079","volume":"89","author":"P Greenberg","year":"1997","unstructured":"Greenberg P, Cox C, LeBeau MM, Fenaux P, Morel P, Sanz G, Sanz M, Vallespi T, Hamblin T, Oscier D, Ohyashiki K, Toyama K, Aul C, Mufti G, Bennett J (1997) International socring system for evaluating prognosis in myelodysplastic syndromes. Blood 89:2079\u20132088","journal-title":"Blood"},{"key":"462_CR41","doi-asserted-by":"crossref","first-page":"188","DOI":"10.1016\/j.cancergencyto.2004.12.019","volume":"160","author":"J Brezinova","year":"2005","unstructured":"Brezinova J, Zemanova Z, Ransdorfova S, Sindelarova L, Siskova M, Neuwirtiva R, Cermak J, Michalova K (2005) Prognostic significance of del(20q) in patients with hematological malignancies. Cancer Genet Cytogenet 160:188\u2013192","journal-title":"Cancer Genet Cytogenet"},{"key":"462_CR42","doi-asserted-by":"crossref","first-page":"174","DOI":"10.1016\/0165-4608(92)90107-J","volume":"58","author":"K Ohyashiki","year":"1992","unstructured":"Ohyashiki K, Murakami T, Ohyashiki JH, Kodama A, Sakai N, Ito H, Toyama K (1992) Double 20q\u2212Anomaly in myelodysplastic syndrome. Cancer Genet Cytogenet 58:174\u2013176","journal-title":"Cancer Genet Cytogenet"},{"key":"462_CR43","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1016\/0165-4608(95)00175-1","volume":"86","author":"I Kubonishi","year":"1996","unstructured":"Kubonishi I, Muneishi H, Hashimoto E, Hatakeyama N, Kuzume T, Miyoshi I (1996) Duplication of del(20)(q11) in a case of MDS. Cancer Genet Cytogenet 86:185\u2013186","journal-title":"Cancer Genet Cytogenet"},{"key":"462_CR44","doi-asserted-by":"crossref","first-page":"680","DOI":"10.1093\/ajcp\/106.5.680","volume":"106","author":"PJ Kurtin","year":"1996","unstructured":"Kurtin PJ, Dewald GW, Shields DJ, Hanson CA (1996) Hematologic disorders associated with deletions of chromosome 20q: a clinicopathologic study of 107 patients. Am J Clin Pathol 106:680\u2013688","journal-title":"Am J Clin Pathol"},{"key":"462_CR45","doi-asserted-by":"crossref","first-page":"219","DOI":"10.1016\/0165-4608(94)90094-9","volume":"78","author":"V Parlier","year":"1994","unstructured":"Parlier V, Van Melle G, Beris P, Schmidt PM, Tobler A, Haller E, Bellomo HJ (1994) Hematologic, clinical, and cytogenetic analysis in 109 patients with primary myelodysplastic syndrome. Prognostic significance of morphology and chromosome findings. Cancer Genet Cytogenet 78:219\u2013231","journal-title":"Cancer Genet Cytogenet"},{"key":"462_CR46","first-page":"67","volume":"8","author":"LJ Campbell","year":"1994","unstructured":"Campbell LJ, Garson OM (1994) The prognostic significance of deletion of the long arm of chromosome 20 in myeloid disorders. Leukemia 8:67\u201371","journal-title":"Leukemia"},{"key":"462_CR47","doi-asserted-by":"crossref","first-page":"407","DOI":"10.1016\/S0145-2126(98)00177-5","volume":"23","author":"D Falzetti","year":"1999","unstructured":"Falzetti D, Vermeesch JR, Hood TL, Nacheva EP, Matteucci C, Martelli MF, Van den Berghe H, Marynen P, Mecucci C (1999) Identification of multiple copies of a 20q\u2212chromosome in a case of myelodysplastic syndrome: a FISH study. Leukemia Research 23:407\u2013413","journal-title":"Leukemia Research"},{"key":"462_CR48","doi-asserted-by":"crossref","first-page":"337","DOI":"10.1111\/j.1365-2141.2004.04921.x","volume":"125","author":"T Li","year":"2004","unstructured":"Li T, Xue Y, Wu Y, Pan J (2004) Clinical and molecular cytogenetic studies in seven patients with myeloid diseases characterized by i(20q\u2212). Br J Haematol 125:337\u2013342","journal-title":"Br J Haematol"}],"container-title":["Annals of Hematology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00277-008-0462-3.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00277-008-0462-3\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00277-008-0462-3","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,5,3]],"date-time":"2020-05-03T06:32:09Z","timestamp":1588487529000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00277-008-0462-3"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,3,19]]},"references-count":48,"journal-issue":{"issue":"7","published-print":{"date-parts":[[2008,7]]}},"alternative-id":["462"],"URL":"https:\/\/doi.org\/10.1007\/s00277-008-0462-3","relation":{},"ISSN":["0939-5555","1432-0584"],"issn-type":[{"value":"0939-5555","type":"print"},{"value":"1432-0584","type":"electronic"}],"subject":[],"published":{"date-parts":[[2008,3,19]]}}}