{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,18]],"date-time":"2026-03-18T00:03:32Z","timestamp":1773792212592,"version":"3.50.1"},"reference-count":20,"publisher":"Oxford University Press (OUP)","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2007,1,1]]},"DOI":"10.1093\/molehr\/gal094","type":"journal-article","created":{"date-parts":[[2006,11,1]],"date-time":"2006-11-01T04:15:04Z","timestamp":1162354504000},"page":"55-59","source":"Crossref","is-referenced-by-count":17,"title":["Sperm-FISH analysis in a pericentric chromosome 1 inversion, 46,XY,inv(1)(p22q42), associated with infertility"],"prefix":"10.1093","volume":"13","author":[{"given":"S.","family":"Chantot-Bastaraud","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Ravel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I.","family":"Berthaut","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"K.","family":"McElreavey","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P.","family":"Bouchard","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.","family":"Mandelbaum","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.P.","family":"Siffroi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2006,10,31]]},"reference":[{"key":"key\n\t\t\t\t20171013135215_ANTON-ET-AL-2002","doi-asserted-by":"crossref","unstructured":"Anton E , Blanco J, Egozcue J and Vidal F (2002) Risk assessment and segregation analysis in a pericentric inversion inv6p23q25 carrier using FISH on decondensed sperm nuclei. Cytogenet Genome Res97,149\u2013154.","DOI":"10.1159\/000066603"},{"key":"key\n\t\t\t\t20171013135215_ANTON-ET-AL-2005","doi-asserted-by":"crossref","unstructured":"Anton E , Blanco J, Egozcue J and Vidal F (2005) Sperm studies in heterozygote inversion carriers: a review. Cytogenet Genome111,297\u2013304.","DOI":"10.1159\/000086903"},{"key":"key\n\t\t\t\t20171013135215_ANTON-ET-AL-2006","doi-asserted-by":"crossref","unstructured":"Anton E , Vidal F, Egozcue J and Blanco J (2006) Genetic reproductive risk in inversion carriers. Fertil Steril85,661\u2013666.","DOI":"10.1016\/j.fertnstert.2005.09.023"},{"key":"key\n\t\t\t\t20171013135215_ASHLEY-1988","doi-asserted-by":"crossref","unstructured":"Ashley T (1988) G-band position effects on meiotic synapsis and crossing over. Genetics118,307\u2013317.","DOI":"10.1093\/genetics\/118.2.307"},{"key":"key\n\t\t\t\t20171013135215_BACHE-ET-AL-2004","doi-asserted-by":"crossref","unstructured":"Bache I , Assche EV, Cingoz S, Bugge M, Tumer Z, Hjorth M, Lundsteen C, Lespinasse J, Winther K, Niebuhr A et al. (2004) An excess of chromosome 1 breakpoints in male infertility. Eur J Hum Genet12,993\u20131000.","DOI":"10.1038\/sj.ejhg.5201263"},{"key":"key\n\t\t\t\t20171013135215_BROWN-ET-AL-1998","doi-asserted-by":"crossref","unstructured":"Brown GM , Leversha M, Hulten M, Ferguson-Smith MA, Affara NA, Furlong RA (1998) Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3. Am J Hum Genet62,1484\u20131492","DOI":"10.1086\/301863"},{"key":"key\n\t\t\t\t20171013135215_DE-LA-ET-AL-1974","unstructured":"de la Chapelle A , Schroder J, Stenstrand K, Fellman J, Herva R, Saarni M, Anttolainen I, Tallila I, Tervila L, Husa L et al. (1974) Pericentric inversions of human chromosomes 9 and 10. Am J Hum Genet26,746\u201366."},{"key":"key\n\t\t\t\t20171013135215_GUTTENBACH-ET-AL-1997","doi-asserted-by":"crossref","unstructured":"Guttenbach M , Engel W and Schmid M (1997) Analysis of structural and numerical chromosome abnormalities in sperm of normal men and carriers of constitutional chromosome aberrations. A review. Hum Genet100,1\u201321.","DOI":"10.1007\/s004390050459"},{"key":"key\n\t\t\t\t20171013135215_JAAROLA-ET-AL-1998","doi-asserted-by":"crossref","unstructured":"Jaarola M , Martin RH and Ashley T (1998) Direct evidence for suppression of recombination within two pericentric inversions in humans: a new sperm-FISH technique. Am J Hum Genet63,218\u2013224.","DOI":"10.1086\/301900"},{"key":"key\n\t\t\t\t20171013135215_KAISER-1984","doi-asserted-by":"crossref","unstructured":"Kaiser P (1984) Pericentric inversions. Problems and significance for clinical genetics. Hum Genet68,1\u201347.","DOI":"10.1007\/BF00293869"},{"key":"key\n\t\t\t\t20171013135215_MALAN-ET-AL-2006","doi-asserted-by":"crossref","unstructured":"Malan V , Pipiras E, Sifer C, Kanafani S, Cedrin-Durnerin I, Martin-Pont B, Hugues JN, Wolf JP and Benzacken B (2006) Chromosome segregation in an infertile man carrying a unique pericentric inversion, inv (21) (p12q22.3), analysed using fluorescence in situ hybridization on sperm nuclei: significance for clinical genetics. A case report. Hum Reprod21,2052\u20132056.","DOI":"10.1093\/humrep\/del090"},{"key":"key\n\t\t\t\t20171013135215_MAU-HOLZMANN-2005","doi-asserted-by":"crossref","unstructured":"Mau-Holzmann UA (2005) Somatic chromosomal abnormalities in infertile men and women. Cytogenet Genome Res111,317\u2013336.","DOI":"10.1159\/000086906"},{"key":"key\n\t\t\t\t20171013135215_MIKHAAIL-PHILIPS-ET-AL-2004","doi-asserted-by":"crossref","unstructured":"Mikhaail-Philips MM , Ko E, Chernos J, Greene C, Rademaker A and Martin RH (2004) Analysis of chromosome segregation in sperm from a chromosome 2 inversion heterozygote and assessment of an interchromosomal effect. Am J Med Genet127,139\u2013143.","DOI":"10.1002\/ajmg.a.20693"},{"key":"key\n\t\t\t\t20171013135215_MIKHAAIL-PHILIPS-ET-AL-2005","doi-asserted-by":"crossref","unstructured":"Mikhaail-Philips MM , McGillivray BC, Hamilton SJ, Ko E, Chernos J, Rademaker A and Martin RH (2005) Unusual segregation products in sperm from a pericentric inversion 17 heterozygote. Hum Genet117,357\u2013365.","DOI":"10.1007\/s00439-004-1245-0"},{"key":"key\n\t\t\t\t20171013135215_MOREL-ET-AL-2006","doi-asserted-by":"crossref","unstructured":"Morel F , Laudier B, Guerif F, Couet ML, Royere D, Roux C, Bresson JL, Amice V, De Braekeleer M and Douet-Guilbert N (2006) Meiotic segregation analysis in spermatozoa of pericentric inversion carriers using fluorescence in-situ hybridization. Hum Reprod August17, 2006 [Epub ahead of print].","DOI":"10.1093\/humrep\/del317"},{"key":"key\n\t\t\t\t20171013135215_NIELSEN-AND-WOHLERT-1991","doi-asserted-by":"crossref","unstructured":"Nielsen J and Wohlert M (1991) Chromosome abnormalities found among 34910 newborn children: results from a 13-year incidence study in Arhus, Denmark. Hum Genet87,81\u201383.","DOI":"10.1007\/BF01213097"},{"key":"key\n\t\t\t\t20171013135215_RAVEL-ET-AL-2006","doi-asserted-by":"crossref","unstructured":"Ravel C , Berthaut I, Bresson JL and Siffroi JP (2006) Prevalence of chromosomal abnormalities in phenotypically normal and fertile adult males: large-scale survey of over 10 000 sperm donor karyotypes. Hum Reprod21,1484\u20131489.","DOI":"10.1093\/humrep\/del024"},{"key":"key\n\t\t\t\t20171013135215_RUBES-ET-AL-2002","doi-asserted-by":"crossref","unstructured":"Rubes J , Vozdova M, Robbins WA, Rezacova O, Perreault SD and Wyrobek AJ (2002) Stable variants of sperm aneuploidy among healthy men show associations between germinal and somatic aneuploidy. Am J Hum Genet70,1507\u20131519.","DOI":"10.1086\/340791"},{"key":"key\n\t\t\t\t20171013135215_WINSOR-ET-AL-1978","doi-asserted-by":"crossref","unstructured":"Winsor EJ , Palmer CG, Ellis PM, Hunter JL and Ferguson-Smith MA (1978) Meiotic analysis of a pericentric inversion, inv (7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7. Cytogenet Cell Genet20,169\u2013184.","DOI":"10.1159\/000130849"},{"key":"key\n\t\t\t\t20171013135215_YAKUT-ET-AL-2003","doi-asserted-by":"crossref","unstructured":"Yakut T , Acar H, Egeli U and Kimya Y (2003) Frequency of recombinant and non recombinant products of pericentric inversion of chromosome 1 in sperm nuclei of carrier: by FISH technique. Mol Reprod Dev66,67\u201371.","DOI":"10.1002\/mrd.10325"}],"container-title":["MHR: Basic science of reproductive medicine"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/academic.oup.com\/molehr\/article-pdf\/13\/1\/55\/3908333\/gal094.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,8,4]],"date-time":"2021-08-04T04:16:55Z","timestamp":1628050615000},"score":1,"resource":{"primary":{"URL":"http:\/\/academic.oup.com\/molehr\/article\/13\/1\/55\/1125080\/SpermFISH-analysis-in-a-pericentric-chromosome-1"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2006,10,31]]},"references-count":20,"journal-issue":{"issue":"1","published-online":{"date-parts":[[2006,10,31]]},"published-print":{"date-parts":[[2007,1,1]]}},"URL":"https:\/\/doi.org\/10.1093\/molehr\/gal094","relation":{},"ISSN":["1460-2407","1360-9947"],"issn-type":[{"value":"1460-2407","type":"electronic"},{"value":"1360-9947","type":"print"}],"subject":[],"published-other":{"date-parts":[[2007,1]]},"published":{"date-parts":[[2006,10,31]]}}}