{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,4,20]],"date-time":"2023-04-20T05:24:29Z","timestamp":1681968269717},"reference-count":45,"publisher":"Springer Science and Business Media LLC","issue":"2","license":[{"start":{"date-parts":[[2015,1,28]],"date-time":"2015-01-28T00:00:00Z","timestamp":1422403200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Chromosome Res"],"published-print":{"date-parts":[[2015,6]]},"DOI":"10.1007\/s10577-015-9465-9","type":"journal-article","created":{"date-parts":[[2015,1,27]],"date-time":"2015-01-27T06:26:35Z","timestamp":1422339995000},"page":"267-276","update-policy":"http:\/\/dx.doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["Decreased XY recombination and disturbed meiotic prophase I progression in an infertile 48, XYY, +sSMC man"],"prefix":"10.1007","volume":"23","author":[{"given":"Liu","family":"Wang","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zhipeng","family":"Xu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Furhan","family":"Iqbal","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Liangwen","family":"Zhong","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yuanwei","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Caiyun","family":"Wu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Guixiang","family":"Zhou","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hanwei","family":"Jiang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ihtisham","family":"Bukhari","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Howard J.","family":"Cooke","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Qinghua","family":"Shi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2015,1,28]]},"reference":[{"issue":"3","key":"9465_CR1","doi-asserted-by":"crossref","first-page":"1041","DOI":"10.1128\/MCB.25.3.1041-1053.2005","volume":"25","author":"WM Baarends","year":"2005","unstructured":"Baarends WM, Wassenaar E, van der Laan R, Hoogerbrugge J, Sleddens-Linkels E, Hoeijmakers JHJ, de Boer P, Grootegoed JA (2005) Silencing of unpaired chromatin and histone H2A ubiquitination in mammalian meiosis. Mol Cell Biol 25(3):1041\u20131053","journal-title":"Mol Cell Biol"},{"key":"9465_CR2","doi-asserted-by":"crossref","first-page":"350","DOI":"10.1038\/sj.ejhg.5200200","volume":"6","author":"AL Barlow","year":"1998","unstructured":"Barlow AL, Hulten MA (1998) Crossing over analysis at pachytene in man. Eur J Hum Genet 6:350\u2013358","journal-title":"Eur J Hum Genet"},{"key":"9465_CR3","doi-asserted-by":"crossref","first-page":"413","DOI":"10.1007\/s004390050381","volume":"99","author":"J Blanco","year":"1997","unstructured":"Blanco J, Rubio C, Simon C, Egozcue J, Vidal F (1997) Increased incidence of disomic sperm nuclei in a 47, XYY male assessed by fluorescent in situ hybridization (FISH). Hum Genet 99:413\u2013416","journal-title":"Hum Genet"},{"key":"9465_CR4","doi-asserted-by":"crossref","first-page":"2017","DOI":"10.1038\/nrg2505","volume":"10","author":"PS Burgoyne","year":"2009","unstructured":"Burgoyne PS, Mahadevaiah SK, Turner JMA (2009) The consequences of asynapsis for mammalian meiosis. Nat Rev Genet 10:2017\u20132216","journal-title":"Nat Rev Genet"},{"key":"9465_CR5","doi-asserted-by":"crossref","first-page":"407","DOI":"10.1007\/s004390050380","volume":"99","author":"E Chevret","year":"1997","unstructured":"Chevret E, Rousseaux S, Monteil M, Usson Y, Cozzi J, Pelletier R, Sele B (1997) Meiotic behaviour of sex chromosomes investigated by three-colour FISH on 35142 sperm nuclei from two 47, XYY males. Hum Genet 99:407\u2013412","journal-title":"Hum Genet"},{"key":"9465_CR6","doi-asserted-by":"crossref","first-page":"2133","DOI":"10.1093\/humrep\/dei023","volume":"20","author":"M Codina-Pascual","year":"2005","unstructured":"Codina-Pascual M, Oliver-Bonet M, Navarro J, Campillo M, Garcia F, Egozcue S, Abad C, Egozcue J, Benet J (2005) Synapsis and meiotic recombination analyses: MLH1 focus in the XY pair as an indicator. Hum Reprod 20:2133\u20132139","journal-title":"Hum Reprod"},{"key":"9465_CR7","doi-asserted-by":"crossref","first-page":"2870","DOI":"10.1093\/hmg\/ddm246","volume":"16","author":"KA Ferguson","year":"2007","unstructured":"Ferguson KA, Wong EC, Chow V, Nigro M, Ma S (2007) Abnormal meiotic recombination in infertile men and its association with sperm aneuploidy. Hum Mol Genet 16:2870\u20132879","journal-title":"Hum Mol Genet"},{"key":"9465_CR8","doi-asserted-by":"crossref","first-page":"154","DOI":"10.1159\/000132314","volume":"43","author":"O Gabrielrobez","year":"1986","unstructured":"Gabrielrobez O, Ratomponirina C, Dutrillaux B, Carrepigeon F, Rumpler Y (1986) Meiotic association between the XY chromosomes and the autosomal quadrivalent of a reciprocal translocation in 2 infertile men, 46, XY, t(19\u201322) and 46, XY, t(17\u201321). Cytogenet Cell Genet 43:154\u2013160","journal-title":"Cytogenet Cell Genet"},{"key":"9465_CR9","first-page":"129","volume":"39","author":"O Gabriel-Robez","year":"1996","unstructured":"Gabriel-Robez O, Delobel B, Croquette MF, Rigot JM, Djlelati R, Rumpler Y (1996) Synaptic behaviour of sex chromosome in two XYY men. Ann Genet 39:129\u2013132","journal-title":"Ann Genet"},{"key":"9465_CR10","doi-asserted-by":"crossref","first-page":"477","DOI":"10.1038\/nrg1614","volume":"6","author":"JL Gerton","year":"2005","unstructured":"Gerton JL, Hawley RS (2005) Homologous chromosome interactions in meiosis: diversity amidst conservation. Nat Rev Genet 6:477\u2013487","journal-title":"Nat Rev Genet"},{"key":"9465_CR11","doi-asserted-by":"crossref","first-page":"2875","DOI":"10.1093\/hmg\/ddh302","volume":"13","author":"J Gonsalves","year":"2004","unstructured":"Gonsalves J, Sun F, Schlegel PN, Turek PJ, Hopps CV, Greene C, Martin RH, Pera RA (2004) Defective recombination in infertile men. Hum Mol Genet 13:2875\u20132883","journal-title":"Hum Mol Genet"},{"key":"9465_CR12","doi-asserted-by":"crossref","first-page":"2409","DOI":"10.1093\/hmg\/9.16.2409","volume":"9","author":"T Hassold","year":"2000","unstructured":"Hassold T, Sherman S, Hunt P (2000) Counting cross-overs: characterizing meiotic recombination in mammals. Hum Mol Genet 9:2409\u20132419","journal-title":"Hum Mol Genet"},{"key":"9465_CR13","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1016\/j.jgg.2014.01.005","volume":"41","author":"H Jiang","year":"2014","unstructured":"Jiang H, Wang L, Cui Y, Xu Z, Guo T, Cheng D, Xu P, Yu W, Shi Q (2014) Meiotic chromosome behavior in a human male t(8;15) carrier. J Genet Genom 41:177\u2013185","journal-title":"J Genet Genom"},{"key":"9465_CR14","doi-asserted-by":"crossref","first-page":"617","DOI":"10.1038\/aja.2009.37","volume":"11","author":"A Koc","year":"2009","unstructured":"Koc A, Onur SO, Ergun MA, Percin EF (2009) Supernumerary marker chromosome 15 in a male with azoospermia and open bite deformity. Asian J Androl 11:617\u2013622","journal-title":"Asian J Androl"},{"key":"9465_CR15","doi-asserted-by":"crossref","first-page":"1","DOI":"10.3389\/fgene.2012.00112","volume":"3","author":"H Kurahashi","year":"2012","unstructured":"Kurahashi H, Kogo H, Tsutsumi M, Inagaki H, Ohye T (2012) Failure of homologous synapsis and sex-specific reproduction problems. Front Genet 3:1\u201311","journal-title":"Front Genet"},{"issue":"1293","key":"9465_CR16","first-page":"e1217","volume":"91","author":"M Leng","year":"2009","unstructured":"Leng M, Li G, Zhong L, Hou H, Yu D, Shi Q (2009) Abnormal synapses and recombination in an azoospermic male carrier of a reciprocal translocation t(1;21). Fertil Steril 91(1293):e1217\u2013e1222","journal-title":"Fertil Steril"},{"key":"9465_CR17","doi-asserted-by":"crossref","first-page":"991","DOI":"10.1369\/jhc.2009.954370","volume":"57","author":"T Liehr","year":"2009","unstructured":"Liehr T (2009) Small supernumerary marker chromosomes (sSMCs): a spotlight on some nomenclature problems. J Histochem Cytochem 57:991\u2013993","journal-title":"J Histochem Cytochem"},{"key":"9465_CR18","first-page":"719","volume":"19","author":"T Liehr","year":"2007","unstructured":"Liehr T, Weise A (2007) Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics. Int J Mol Med 19:719\u2013731","journal-title":"Int J Mol Med"},{"key":"9465_CR19","doi-asserted-by":"crossref","first-page":"55","DOI":"10.1159\/000079572","volume":"107","author":"T Liehr","year":"2004","unstructured":"Liehr T, Claussen U, Starke H (2004) Small supernumerary marker chromosomes (sSMC) in humans. Cytogenet Genome Res 107:55\u201367","journal-title":"Cytogenet Genome Res"},{"key":"9465_CR20","doi-asserted-by":"crossref","first-page":"23","DOI":"10.1159\/000087510","volume":"112","author":"T Liehr","year":"2006","unstructured":"Liehr T et al (2006) Small supernumerary marker chromosomes\u2014progress towards a genotype-phenotype correlation. Cytogenet Genome Res 112:23\u201334","journal-title":"Cytogenet Genome Res"},{"key":"9465_CR21","doi-asserted-by":"crossref","first-page":"182","DOI":"10.1073\/pnas.69.1.182","volume":"69","author":"E Lifschyt","year":"1972","unstructured":"Lifschyt E, Lindsley DL (1972) Role of X-chromosome inactivation during spermatogenesis. Proc Natl Acad Sci U S A 69:182","journal-title":"Proc Natl Acad Sci U S A"},{"key":"9465_CR22","doi-asserted-by":"crossref","first-page":"468","DOI":"10.1016\/0029-7844(95)00419-X","volume":"87","author":"MG Linden","year":"1996","unstructured":"Linden MG, Bender BG, Robinson A (1996) Intrauterine diagnosis of sex chromosome aneuploidy. Obstet Gynecol 87:468\u2013475","journal-title":"Obstet Gynecol"},{"key":"9465_CR23","doi-asserted-by":"crossref","first-page":"980","DOI":"10.1093\/humrep\/dei428","volume":"21","author":"S Ma","year":"2006","unstructured":"Ma S, Ferguson KA, Arsovska S, Moens P, Chow V (2006) Reduced recombination associated with the production of aneuploid sperm in an infertile man: a case report. Hum Reprod 21:980\u2013985","journal-title":"Hum Reprod"},{"key":"9465_CR24","doi-asserted-by":"crossref","first-page":"271","DOI":"10.1038\/85830","volume":"27","author":"SK Mahadevaiah","year":"2001","unstructured":"Mahadevaiah SK, Turner JM, Baudat F, Rogakou EP, de Boer P, Blanco-Rodriguez J, Jasin M, Keeney S, Bonner WM, Burgoyne PS (2001) Recombinational DNA double-strand breaks in mice precede synapsis. Nat Genet 27:271\u2013276","journal-title":"Nat Genet"},{"key":"9465_CR25","doi-asserted-by":"crossref","first-page":"233","DOI":"10.1111\/cge.12138","volume":"85","author":"N Marle","year":"2014","unstructured":"Marle N et al (2014) Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective study. Clin Genet 85:233\u2013244","journal-title":"Clin Genet"},{"key":"9465_CR26","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1017\/S0967199499000489","volume":"7","author":"RH Martin","year":"1999","unstructured":"Martin RH, McInnes B, Rademaker AW (1999) Analysis of aneuploidy for chromosomes 13, 21, X and Y by multicolour fluorescence in situ hybridisation (FISH) in a 47, XYY male. Zygote 7:131\u2013134","journal-title":"Zygote"},{"key":"9465_CR27","doi-asserted-by":"crossref","first-page":"165","DOI":"10.1016\/j.bbaexp.2003.11.017","volume":"1677","author":"BD McKee","year":"2004","unstructured":"McKee BD (2004) Homologous pairing and chromosome dynamics in meiosis and mitosis. Biochim Biophys Acta 1677:165\u2013180","journal-title":"Biochim Biophys Acta"},{"key":"9465_CR28","first-page":"11","volume":"20","author":"K Mennicke","year":"1997","unstructured":"Mennicke K, Diercks P, Schlieker H, Bals-Pratsch M, Al Hasani S, Diedrich K, Schwinger E (1997) Molecular cytogenetic diagnostics in sperm. Int J Androl 20:11\u201319","journal-title":"Int J Androl"},{"key":"9465_CR29","doi-asserted-by":"crossref","first-page":"88","DOI":"10.1002\/ajmg.1320460115","volume":"46","author":"K Michalski","year":"1993","unstructured":"Michalski K, Rauer M, Williamson N, Perszyk A, Hoo JJ (1993) Identification, counselling, and outcome of two cases of prenatally diagnosed supernumerary small ring chromosomes. Am J Med Genet 46:88\u201394","journal-title":"Am J Med Genet"},{"key":"9465_CR30","doi-asserted-by":"crossref","first-page":"376","DOI":"10.1093\/oxfordjournals.humrep.a137343","volume":"6","author":"J Navarro","year":"1991","unstructured":"Navarro J, Vidal F, Benet J, Templado C, Marina S, Egozcue J (1991) XY trivalent association and synaptic anomalies in a male carrier of a Robertsonian T(13, 14) translocation. Hum Reprod 6:376\u2013381","journal-title":"Hum Reprod"},{"key":"9465_CR31","doi-asserted-by":"crossref","first-page":"581","DOI":"10.1002\/ajmg.a.35222","volume":"158A","author":"ZZ Pan","year":"2012","unstructured":"Pan ZZ, Yang QL, Ye N, Wang L, Li JH, Yu DX, Cooke HJ, Shi QH (2012) Complex relationship between meiotic recombination frequency and autosomal synaptonemal complex length per cell in normal human males. Am J Med Genet A 158A:581\u2013587","journal-title":"Am J Med Genet A"},{"key":"9465_CR32","doi-asserted-by":"crossref","first-page":"242","DOI":"10.1046\/j.1365-2605.2003.00421.x","volume":"26","author":"N Rives","year":"2003","unstructured":"Rives N, Simeon N, Milazzo JP, Barthelemy C, Mace B (2003) Meiotic segregation of sex chromosomes in mosaic and non-mosaic XYY males: case reports and review of the literature. Int J Androl 26:242\u2013249","journal-title":"Int J Androl"},{"key":"9465_CR33","doi-asserted-by":"crossref","first-page":"2205","DOI":"10.1093\/hmg\/8.12.2205","volume":"8","author":"DO Robinson","year":"1999","unstructured":"Robinson DO, Jacobs PA (1999) The origin of the extra Y chromosome in males with a 47, XYY karyotype. Hum Mol Genet 8:2205\u20132209","journal-title":"Hum Mol Genet"},{"key":"9465_CR34","doi-asserted-by":"crossref","first-page":"1194","DOI":"10.1093\/humrep\/dei479","volume":"21","author":"RB Sciurano","year":"2006","unstructured":"Sciurano RB, Rahn MI, Pigozzi MI, Olmedo SB, Solari AJ (2006) An azoospermic man with a double-strand DNA break-processing deficiency in the spermatocyte nuclei: case report. Hum Reprod 21:1194\u20131203","journal-title":"Hum Reprod"},{"key":"9465_CR35","doi-asserted-by":"crossref","first-page":"142","DOI":"10.1093\/humrep\/del330","volume":"22","author":"R Sciurano","year":"2007","unstructured":"Sciurano R, Rahn M, Rey-Valzacchi G, Solari AJ (2007) The asynaptic chromatin in spermatocytes of translocation carriers contains the histone variant gamma-H2AX and associates with the XY body. Hum Reprod 22:142\u2013150","journal-title":"Hum Reprod"},{"key":"9465_CR36","doi-asserted-by":"crossref","first-page":"655","DOI":"10.1530\/rep.0.1210655","volume":"121","author":"Q Shi","year":"2001","unstructured":"Shi Q, Martin RH (2001) Aneuploidy in human spermatozoa: FISH analysis in men with constitutional chromosomal abnormalities, and in infertile men. Reproduction 121:655\u2013666","journal-title":"Reproduction"},{"key":"9465_CR37","doi-asserted-by":"crossref","first-page":"34","DOI":"10.1002\/1096-8628(20010215)99:1<34::AID-AJMG1106>3.0.CO;2-D","volume":"99","author":"QH Shi","year":"2001","unstructured":"Shi QH, Spriggs E, Field LL, Ko E, Barclay L, Martin RH (2001) Single sperm typing demonstrates that reduced recombination is associated with the production of aneuploid 24, XY human sperm. Am J Med Genet 99:34\u201338","journal-title":"Am J Med Genet"},{"key":"9465_CR38","doi-asserted-by":"crossref","first-page":"467","DOI":"10.1023\/A:1018469030537","volume":"5","author":"AJ Solari","year":"1997","unstructured":"Solari AJ, Rey Valzacchi G (1997) The prevalence of a YY synaptonemal complex over XY synapsis in an XYY man with exclusive XYY spermatocytes. Chromosom Res 5:467\u2013474","journal-title":"Chromosom Res"},{"key":"9465_CR39","doi-asserted-by":"crossref","first-page":"521","DOI":"10.1086\/382138","volume":"74","author":"F Sun","year":"2004","unstructured":"Sun F, Oliver-Bonet M, Liehr T, Starke H, Ko E, Rademaker A, Navarro J, Benet J, Martin RH (2004) Human male recombination maps for individual chromosomes. Am J Hum Genet 74:521\u2013531","journal-title":"Am J Hum Genet"},{"key":"9465_CR40","doi-asserted-by":"crossref","first-page":"399","DOI":"10.1093\/molehr\/gan030","volume":"14","author":"F Sun","year":"2008","unstructured":"Sun F, Mikhaail-Philips M, Oliver-Bonet M, Ko E, Rademaker A, Turek P, Martin RH (2008) Reduced meiotic recombination on the XY bivalent is correlated with an increased incidence of sex chromosome aneuploidy in men with non-obstructive azoospermia. Mol Hum Reprod 14:399\u2013404","journal-title":"Mol Hum Reprod"},{"key":"9465_CR41","doi-asserted-by":"crossref","first-page":"3171","DOI":"10.1093\/humrep\/del281","volume":"21","author":"D Topping","year":"2006","unstructured":"Topping D, Brown P, Judis L, Schwartz S, Seftel A, Thomas A, Hassold T (2006) Synaptic defects at meiosis I and non-obstructive azoospermia. Hum Reprod 21:3171\u20133177","journal-title":"Hum Reprod"},{"key":"9465_CR42","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1186\/1755-8166-1-7","volume":"1","author":"KD Tsuchiya","year":"2008","unstructured":"Tsuchiya KD, Opheim KE, Hannibal MC, Hing AV, Glass IA, Raff ML, Norwood T, Torchia BA (2008) Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridization. Mol Cytogenet 1:7","journal-title":"Mol Cytogenet"},{"key":"9465_CR43","doi-asserted-by":"crossref","first-page":"2135","DOI":"10.1016\/j.cub.2004.11.032","volume":"14","author":"JM Turner","year":"2004","unstructured":"Turner JM, Aprelikova O, Xu X, Wang R, Kim S, Chandramouli GV, Barrett JC, Burgoyne PS, Deng CX (2004) BRCA1, histone H2AX phosphorylation, and male meiotic sex chromosome inactivation. Curr Biol 14:2135\u20132142","journal-title":"Curr Biol"},{"key":"9465_CR44","doi-asserted-by":"crossref","first-page":"41","DOI":"10.1038\/ng1484","volume":"37","author":"JM Turner","year":"2005","unstructured":"Turner JM, Mahadevaiah SK, Fernandez-Capetillo O, Nussenzweig A, Xu X, Deng CX, Burgoyne PS (2005) Silencing of unsynapsed meiotic chromosomes in the mouse. Nat Genet 37:41\u201347","journal-title":"Nat Genet"},{"key":"9465_CR45","first-page":"171","volume":"27","author":"WR Yu","year":"1995","unstructured":"Yu WR, Gabriel-Robez O, Croquette MF, Rigot JM, Rumpler Y (1995) XY-quadrivalent association and sterility in a man carrier of a reciprocal autosomal translocation involving the whole arm of an acrocentric chromosome t(2;15)(q21.3;cen). Andrologia 27:171\u2013174","journal-title":"Andrologia"}],"container-title":["Chromosome Research"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10577-015-9465-9.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s10577-015-9465-9\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10577-015-9465-9","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,8,20]],"date-time":"2019-08-20T00:55:37Z","timestamp":1566262537000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s10577-015-9465-9"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,1,28]]},"references-count":45,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2015,6]]}},"alternative-id":["9465"],"URL":"https:\/\/doi.org\/10.1007\/s10577-015-9465-9","relation":{},"ISSN":["0967-3849","1573-6849"],"issn-type":[{"value":"0967-3849","type":"print"},{"value":"1573-6849","type":"electronic"}],"subject":[],"published":{"date-parts":[[2015,1,28]]}}}