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Therman E, Susman B, Denniston C. The nonrandom participation of human acrocentric chromosomes in Robertsonian translocations. Ann Hum Genet. 1989; 53(1): 49-65.ThermanESusmanBDennistonC.The nonrandom participation of human acrocentric chromosomes in Robertsonian translocations19895314965Search in Google Scholar
Luciani JM, Guichaoua MR, Mattei A, Morazzani MR. Pachytene analysis of a man with a 13q;14q translocation and infertility. Cytogenet Cel Genet. 1984; 38(1): 14-22.LucianiJMGuichaouaMRMatteiAMorazzaniMR.Pachytene analysis of a man with a 13q;14q translocation and infertility19843811422Search in Google Scholar
Cassuto NG, Le Foll N, Chantot-Bastaraud S, Balet R, Bouret D, Rouen A, et al. Sperm fluorescence in situ hybridization study in nine men carrying a Robertsonian or a reciprocal translocation: Relationship between segregation modes and high-magnification sperm morphology examination. Fertil Steril. 2011; 96(4): 826-832.CassutoNGLe FollNChantot-BastaraudSBaletRBouretDRouenASperm fluorescence in situ hybridization study in nine men carrying a Robertsonian or a reciprocal translocation: Relationship between segregation modes and high-magnification sperm morphology examination2011964826832Search in Google Scholar
Sybenga J. Chromosome structural variants. In: Sybenga J, Ed. General Cytogenetics. Amsterdam, The Netherlands: North-Holland Publishing Company 1975: 165-212.SybengaJ.Chromosome structural variantsSyb***engaJAmsterdam, The NetherlandsNorth-Holland Publishing Company1975165212Search in Google Scholar
Roux C, Tripogney C, Morel F, Joanne C, Fellmann F, Clavequin MC, et al. Segregation of chromosomes in sperm of Robertsonian translocation carriers. Cytogenet Genome Res. 2005; 111(3-4): 291-296.RouxCTripogneyCMorelFJoanneCFellmannFClavequinMCSegregation of chromosomes in sperm of Robertsonian translocation carriers20051113-4291296Search in Google Scholar
Rives N, Ravel C, Duchesne V, Siffroi JP, Mousset-Simeon N, Mace B. Molecular cytogenetics analysis with whole chromosome paint probes of sperm nuclei from a (13;15) Robertsonian translocation carrier. J Hum Genet. 2005; 50(7): 360-364.RivesNRavelCDuchesneVSiffroiJPMousset-SimeonNMaceB.Molecular cytogenetics analysis with whole chromosome paint probes of sperm nuclei from a (13;15) Robertsonian translocation carrier2005507360364Search in Google Scholar
Anahory T, Hamamah S, Andreo B, Hedon B, Claustres M, Sarda P, et al. Sperm segregation analysis of a (13;22) Robertsonian translocation carrier by FISH: A comparison of locus-specific probe and whole chromosome painting. Hum Reprod. 2005; 20(7): 1850-1854.AnahoryTHamamahSAndreoBHedonBClaustresMSardaPSperm segregation analysis of a (13;22) Robertsonian translocation carrier by FISH: A comparison of locus-specific probe and whole chromosome painting200520718501854Search in Google Scholar
Moradkhani K, Puechberty J, Bhatt S, Vago P, Janny L, Lefort G, et al. Meiotic segregation of rare Rob-ertsonian translocations: Sperm analysis of three t(14q; 22q) cases. Hum Reprod. 2006; 21(5): 1166-1171.MoradkhaniKPuechbertyJBhattSVagoPJannyLLefortGMeiotic segregation of rare Rob-ertsonian translocations: Sperm analysis of three t(14q; 22q) cases200621511661171Search in Google Scholar
Anton E, Vidal F, Blanco J. Role of sperm FISH studies in the genetic reproductive advice of structural reorganization carriers. Hum Reprod. 2007; 22(8): 2088-2092.AntonEVidalFBlancoJ.Role of sperm FISH studies in the genetic reproductive advice of structural reorganization carriers200722820882092Search in Google Scholar
Liu Y, Zhu H. Detection of sperm chromosomes in Robertsonian translocation carriers by dual-color fluorescence in situ hybridization. Zhonghua Nan Ke Xue. 2004; 10(2): 90-93.LiuYZhuH.Detection of sperm chromosomes in Robertsonian translocation carriers by dual-color fluorescence in situ hybridization20041029093Search in Google Scholar
Lejeune J. Autosomal disorders. Pediatrics. 1963; 32(3): 326-337.LejeuneJ.Autosomal disorders1963323326337Search in Google Scholar
Douet-Guilbert N, Bris MJ, Amice V, Marchetti C, Delobel B, Amice J, et al. Interchromosomal effect in sperm of males with translocations: Report of 6 cases and review of the literature. Int J Androl. 2005; 28(6): 372-379.Douet-GuilbertNBrisMJAmiceVMarchettiCDelobelBAmiceJInterchromosomal effect in sperm of males with translocations: Report of 6 cases and review of the literature2005286372379Search in Google Scholar
Ogur G, Van Assche E, Vegetti W, Verheyen G, Tournaye H, Bonduelle M, et al. Chromosomal segregation in spermatozoa of 14 Robertsonian translocation carriers. Mol Hum Reprod. 2006; 12(3): 209-215.OgurGVan AsscheEVegettiWVerheyenGTournayeHBonduelleMChromosomal segregation in spermatozoa of 14 Robertsonian translocation carriers2006123209215Search in Google Scholar
Estop AM, Cieply K, Munne S, Surti U, Wakim A, Feingold E. Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies. Hum Genet. 2000; 106(5): 517-524.EstopAMCieplyKMunneSSurtiUWakimAFeingoldE.Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies20001065517524Search in Google Scholar
Acar H, Yildirim MS, Cora T, Ceylaner S. Evaluation of segregation patterns of 21;21 Robertsonian translocation along with sex chromosomes and interchromosomal effects in sperm nuclei of carrier by FISH technique. Mol Reprod Dev. 2002; 63(2): 232-236.AcarHYildirimMSCoraTCeylanerS.Evaluation of segregation patterns of 21;21 Robertsonian translocation along with sex chromosomes and interchromosomal effects in sperm nuclei of carrier by FISH technique2002632232236Search in Google Scholar
World Health Organisation. WHO Laboratory Manual for the Examination and Processing of Human Semen, 5th ed. Geneva, Switzerland, 2010.World Health Organisation5thGenevaSwitzerland2010Search in Google Scholar
Machev N, Gosset P, Warter S, Treger M, Schillinger M, Viville S. Fluorescence in situ hybridization sperm analysis of six translocation carriers provides evidence of an interchromosomal effect. Fertil Steril. 2005; 84(2): 365-373.MachevNGossetPWarterSTregerMSchillingerMVivilleS.Fluorescence in situ hybridization sperm analysis of six translocation carriers provides evidence of an interchromosomal effect2005842365373Search in Google Scholar
Mahjoub M, Mehdi M, Brahem S, Elghezal H, Ibala S, Saad A. Chromosomal segregation in spermatozoa of five Robertsonian translocation carriers t(13;14). J Assist Reprod Genet. 2011; 28(7): 607-613.MahjoubMMehdiMBrahemSElghezalHIbalaSSaadA.Chromosomal segregation in spermatozoa of five Robertsonian translocation carriers t(13;14)2011287607613Search in Google Scholar
Rouen A, Pyram K, Pollet-Villard X, Hyon C, Dorna M, Marques S, et al. Simultaneous cell by cell study of both DNA fragmentation and chromosomal segregation in spermatozoa from chromosomal rearrangement carriers. J Assist Reprod Genet. 2013;30(3):383-390. 10.1007/s10815-012-9915-7.RouenAPyramKPollet-VillardXHyonCDornaMMarquesSSimultaneous cell by cell study of both DNA fragmentation and chromosomal segregation in spermatozoa from chromosomal rearrangement carriers201330338339010.1007/s10815-012-9915-7Open DOISearch in Google Scholar
Ferfouri F, Selva J, Boitrelle F, Gomes DM, Torre A, AlbertM, et al. The chromosomal risk in sperm from heterozygous Robertsonian translocation carriers is related to the sperm count and the translocation type. Fertil Steril. 2011; 96(6): 1337-1343.FerfouriFSelvaJBoitrelleFGomesDMTorreAAlbertMThe chromosomal risk in sperm from heterozygous Robertsonian translocation carriers is related to the sperm count and the translocation type201196613371343Search in Google Scholar
Kovac JR, Pastuszak AW, Lamb DJ. The use of genomics, proteomics, and metabolomics in identifying biomarkers of male infertility. Fertil Steril. 2013; 99(4): 998-1007.KovacJRPastuszakAWLambDJ.The use of genomics, proteomics, and metabolomics in identifying biomarkers of male infertility20139949981007Search in Google Scholar
Luciani JM, Guichaoua MR, Mattei A, Morazzani MR. Pachytene analysis of a man with a 13q;14q translocation and infertility. Behavior of the trivalent and nonrandom association with the sex vesicle. Cytogenet Cell Genet. 1984; 38(1): 14-22.LucianiJMGuichaouaMRMatteiAMorazzaniMR.Pachytene analysis of a man with a 13q;14q translocation and infertility. Behavior of the trivalent and nonrandom association with the sex vesicle19843811422Search in Google Scholar
Navarro J, Vidal F, Benet J, Templado C, Marinas Egozcue J. XY-trivalent association and synaptic anomalies in a male carrier of a Robertsonian t(13;14) translocation. Hum Reprod. 1991; 6(3): 376-381.NavarroJVidalFBenetJTempladoCMarinas EgozcueJ.XY-trivalent association and synaptic anomalies in a male carrier of a Robertsonian t(13;14) translocation199163376381Search in Google Scholar
Morel F, Douet-Guilbert N, Le Bris MJ, Herry A, Amice V, Amice J, et al. Meiotic segregation of translocations during male gametogenesis. Int J Androl. 2004; 27(4): 200-212.MorelFDouet-GuilbertNLe BrisMJHerryAAmiceVAmiceJMeiotic segregation of translocations during male gametogenesis2004274200212Search in Google Scholar
Dallapiccola B, Ferranti G, Altissimi D, Colloridi F, Paesano R. First-trimester prenatal diagnosis of homozygous (14;21) translocation in a fetus with 44 chromosomes. Prenat Diagn. 1989; 9(8): 555-558.DallapiccolaBFerrantiGAltissimiDColloridiFPaesanoR.First-trimester prenatal diagnosis of homozygous (14;21) translocation in a fetus with 44 chromosomes198998555558Search in Google Scholar
Martinez-Castro P, Ramos MC, Rey JA, Benitez J, Sanchez Cascos A. Homozygosity for a Robertsonian-translocation (13q14q) in three offspring of heterozygous parents. Cytogenet Cell Genet. 1984; 38(4): 310-312.Martinez-CastroPRamosMCReyJABenitezJSanchez CascosA.Homozygosity for a Robertsonian-translocation (13q14q) in three offspring of heterozygous parents1984384310312Search in Google Scholar
Rajangam S, Michaelis RC, Velagaleti GV, Lincoln S, Hegde S, Lewin S, et al. Down syndrome with biparental inheritance of der(14q21q) and maternally derived trisomy 21: Confirmation by fluorescent in situ hybridization and microsatellite polymorphism analysis. Am J Med Genet Part A. 1997; 70(1): 43-47.RajangamSMichaelisRCVelagaletiGVLincolnSHegdeSLewinSDown syndrome with biparental inheritance of der(14q21q) and maternally derived trisomy 21: Confirmation by fluorescent in situ hybridization and microsatellite polymorphism analysis19977014347Search in Google Scholar
Wang W, Lan H. Rapid and parallel chromosomal number reductions in muntjac deer inferred from mitochondrial DNA phylogeny. Mol Biol Evol. 2000; 17(9): 1326-1333.WangWLanH.Rapid and parallel chromosomal number reductions in muntjac deer inferred from mitochondrial DNA phylogeny200017913261333Search in Google Scholar
Lindenbaum RH, Hulten M, McDermott A, Seabright M. The prevalence of translocations in parents of children with regular trisomy 21: A possible interchromosomal effect? J Med Genet. 1985; 22(1): 24-28.LindenbaumRHHultenMMcDermottASeabrightM.The prevalence of translocations in parents of children with regular trisomy 21: A possible interchromosomal effect?19852212428Search in Google Scholar
Britton-Davidian J, Catalan J, da Graça Ramalhinho M, Ganem G, Auffray JC, Capela R, et al. Rapid chromosomal evolution in island mice. Nature. 2000; 403(6766): 158.Britton-DavidianJCatalanJda Graça RamalhinhoMGanemGAuffrayJCCapelaRRapid chromosomal evolution in island mice20004036766158Search in Google Scholar
Bint SM, Makie Ogilvie C, Flinter FA, Khalaf Y, Scriven PN. Meiotic segregation of Robertsonian translocations ascertained in cleavage-stage embryos — Implications for preimplantation genetic diagnosis. Hum Reprod. 2011: 26(6): 1575-1584.BintSMMakie OgilvieCFlinterFAKhalafYScrivenPN.Meiotic segregation of Robertsonian translocations ascertained in cleavage-stage embryos — Implications for preimplantation genetic diagnosis201126615751584Search in Google Scholar
Bernicot I, Schneider A, Mace A, Hamamah S, Hedon B, Pellestor F, et al. Analysis using fish of sperm and embryos from two carriers of rare rob(13;21) and rob(15; 22) robertsonian translocation undergoing PGD. Eur J Med Genet. 2012; 55(4?): 245-251.BernicotISchneiderAMaceAHamamahSHedonBPellestorFAnalysis using fish of sperm and embryos from two carriers of rare rob(13;21) and rob(15; 22) robertsonian translocation undergoing PGD2012554?245251Search in Google Scholar
Fischer J, Colls P, Escudero T, Munne S. Preim-plantation genetic diagnosis (PGD) improves pregnancy outcome for translocation carriers with a history of recurrent losses. Fertil Steril. 2010; 94(1): 283-289.FischerJCollsPEscuderoTMunneS.Preim-plantation genetic diagnosis (PGD) improves pregnancy outcome for translocation carriers with a history of recurrent losses2010941283289Search in Google Scholar
Jin H, Ping L, Jie Q, Ying L, Jongjian C. Translocation chromosome karyotypes of the Robertsonian trans-location carriers’ embryos. Fertil Steril. 2010; 93(4): 1061-1065.JinHPingLJieQYingLJongjianC.Translocation chromosome karyotypes of the Robertsonian trans-location carriers’ embryos201093410611065Search in Google Scholar
John B. Chromosome change and evolutionary change: A critique. In: Atchley WR, Woodruff DS, Eds. Evolution and Specification: Essays in Honor of M.J.D. White. London, UK: Cambridge University Press. 1981: 23-51.JohnB.Chromosome change and evolutionary change: A critiqueAtchleyWRWoodruffDSLondon, UKCambridge University Press19812351Search in Google Scholar
Wang B, Xia Y, Song J, Wang W, Tang Y. Potential speciation in humans involving Robertsonian translocations. Biomed Res. 2013; 24(1): 171-174WangBXiaYSongJWangWTangY.Potential speciation in humans involving Robertsonian translocations2013241171174Search in Google Scholar