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Wesselink AK, Wise LA, Hatch EE, Mikkelsen EM, Savitz DA, Kirwa K, et al. A Prospective Cohort Study of Seasonal Variation in Spontaneous Abortion. Epidemiology. 2022; 33(3): 441–448.WesselinkAKWiseLAHatchEEMikkelsenEMSavitzDAKirwaKA Prospective Cohort Study of Seasonal Variation in Spontaneous AbortionEpidemiology2022333441448Search in Google Scholar
Schmidt-Hansen M, Cameron S, Lord J, Hasler E. Initiation of abortion before there is definitive ultrasound evidence of intrauterine pregnancy: A systematic review with meta-analyses. Acta Obstet Gynecol Scand. 2020; 99(4): 451–458.Schmidt-HansenMCameronSLordJHaslerEInitiation of abortion before there is definitive ultrasound evidence of intrauterine pregnancy: A systematic review with meta-analysesActa Obstet Gynecol Scand2020994451458Search in Google Scholar
Woolner AMF, Raja EA, Bhattacharya S, Danielian P, Bhattacharya S. Inherited susceptibility to miscarriage: a nested case-control study of 31,565 women from an intergenerational cohort. Am J Obstet Gynecol. 2020; 222: 168.e1–168.e8.WoolnerAMFRajaEABhattacharyaSDanielianPBhattacharyaSInherited susceptibility to miscarriage: a nested case-control study of 31,565 women from an intergenerational cohortAm J Obstet Gynecol2020222168.e1168.e8Search in Google Scholar
Rolnik DL, Carvalho MH, Catelani AL, Pinto AP, Lira JB, Kusagari NK, et al. [Cytogenetic analysis of miscarriage material from spontaneous abortion]. Rev Assoc Med Bras. 2010; 56(6): 681–683.RolnikDLCarvalhoMHCatelaniALPintoAPLiraJBKusagariNK[Cytogenetic analysis of miscarriage material from spontaneous abortion]Rev Assoc Med Bras2010566681683Search in Google Scholar
Kim JW, Lyu SW, Sung SR, Park JE, Cha DH, Yoon TK, et al. Molecular analysis of miscarriage products using multiplex ligation-dependent probe amplification (MLPA): alternative to conventional karyotype analysis. Arch Gynecol Obstet. 2015; 291(2): 347–354.KimJWLyuSWSungSRParkJEChaDHYoonTKMolecular analysis of miscarriage products using multiplex ligation-dependent probe amplification (MLPA): alternative to conventional karyotype analysisArch Gynecol Obstet20152912347354Search in Google Scholar
Carp H, Toder V, Aviram A, Daniely M, Mashiach S, Barkai G. Karyotype of the abortus in recurrent miscarriage. Fertil Steril. 2001; 75(4): 678–682.CarpHToderVAviramADanielyMMashiachSBarkaiGKaryotype of the abortus in recurrent miscarriageFertil Steril2001754678682Search in Google Scholar
Pinar MH, Gibbins K, He M, Kostadinov S, Silver R. Early Pregnancy Losses: Review of Nomenclature, Histopathology, and Possible Etiologies. Fetal Pediatr Pathol. 2018; 37(3): 191–209.PinarMHGibbinsKHeMKostadinovSSilverREarly Pregnancy Losses: Review of Nomenclature, Histopathology, and Possible EtiologiesFetal Pediatr Pathol2018373191209Search in Google Scholar
Colley E, Hamilton S, Smith P, Morgan NV, Coomarasamy A, Allen S. Potential genetic causes of miscarriage in euploid pregnancies: a systematic review. Hum Reprod Update. 2019; 25(4): 452–472.ColleyEHamiltonSSmithPMorganNVCoomarasamyAAllenSPotential genetic causes of miscarriage in euploid pregnancies: a systematic reviewHum Reprod Update2019254452472Search in Google Scholar
Ljunger E, Cnattingius S, Lundin C, Annerén G. Chromosomal anomalies in first-trimester miscarriages. Acta Obstet Gynecol Scand. 2005; 84(11): 1103–1107.LjungerECnattingiusSLundinCAnnerénGChromosomal anomalies in first-trimester miscarriagesActa Obstet Gynecol Scand2005841111031107Search in Google Scholar
Du Y, Chen L, Lin J, Zhu J, Zhang N, Qiu X, et al. Chromosomal karyotype in chorionic villi of recurrent spontaneous abortion patients. Biosci Trends. 2018; 12(1): 32–39.DuYChenLLinJZhuJZhangNQiuXChromosomal karyotype in chorionic villi of recurrent spontaneous abortion patientsBiosci Trends20181213239Search in Google Scholar
Robinson WP, McFadden DE, Stephenson MD. The origin of abnormalities in recurrent aneuploidy/polyploidy. Am J Hum Genet. 2001; 69(6): 1245–1254.RobinsonWPMcFaddenDEStephensonMDThe origin of abnormalities in recurrent aneuploidy/polyploidyAm J Hum Genet200169612451254Search in Google Scholar
Nguyen BT, Chang EJ, Bendikson KA. Advanced paternal age and the risk of spontaneous abortion: an analysis of the combined 2011–2013 and 2013–2015 National Survey of Family Growth. Am J Obstet Gynecol. 2019; 221(5): 476.e1–476.e7.NguyenBTChangEJBendiksonKAAdvanced paternal age and the risk of spontaneous abortion: an analysis of the combined 2011–2013 and 2013–2015 National Survey of Family GrowthAm J Obstet Gynecol20192215476.e1476.e7Search in Google Scholar
Jia CW, Wang L, Lan YL, Song R, Zhou LY, Yu L, et al. Aneuploidy in Early Miscarriage and its Related Factors. Chin Med J (Engl). 2015; 128(20): 2772–2776.JiaCWWangLLanYLSongRZhouLYYuLAneuploidy in Early Miscarriage and its Related FactorsChin Med J (Engl)20151282027722776Search in Google Scholar
Toufaily MH, Roberts DJ, Westgate MN, Holmes LB. Triploidy: Variation of Phenotype. Am J Clin Pathol. 2016; 145(1): 86–95.ToufailyMHRobertsDJWestgateMNHolmesLBTriploidy: Variation of PhenotypeAm J Clin Pathol201614518695Search in Google Scholar
Wada Y, Kakiuchi S, Mizuguchi K, Nakamura T, Ito Y, Sago H, et al. A female newborn having mosaicism with near-tetraploidy and trisomy 18. Am J Med Genet A. 2016; 170A(5): 1262–1267.WadaYKakiuchiSMizuguchiKNakamuraTItoYSagoHA female newborn having mosaicism with near-tetraploidy and trisomy 18Am J Med Genet A2016170A512621267Search in Google Scholar
Shah MS, Cinnioglu C, Maisenbacher M, Comstock I, Kort J, Lathi RB. Comparison of cytogenetics and molecular karyotyping for chromosome testing of miscarriage specimens. Fertil Steril. 2017; 107(4): 1028–1033.ShahMSCinniogluCMaisenbacherMComstockIKortJLathiRBComparison of cytogenetics and molecular karyotyping for chromosome testing of miscarriage specimensFertil Steril2017107410281033Search in Google Scholar
Magnus MC, Hockey RL, Håberg SE, Mishra GD. Pre-pregnancy lifestyle characteristics and risk of miscarriage: the Australian Longitudinal Study on Women’s Health. BMC Pregnancy Childbirth. 2022; 22(1): 169.MagnusMCHockeyRLHåbergSEMishraGDPre-pregnancy lifestyle characteristics and risk of miscarriage: the Australian Longitudinal Study on Women’s HealthBMC Pregnancy Childbirth2022221169Search in Google Scholar
Bastos R, Ramalho C, Dória S. [Prevalence of chromosomal abnormalities in spontaneous abortions or fetal deaths]. Acta Med Port. 2014; 27(1): 42–48.BastosRRamalhoCDóriaS[Prevalence of chromosomal abnormalities in spontaneous abortions or fetal deaths]Acta Med Port20142714248Search in Google Scholar
Babu R, Van Dyke DL, Bhattacharya S, Dev VG, Liu M, Kwon M, et al. A rapid and reliable chromosome analysis method for products of conception using interphase nuclei. Mol Genet Genomic Med. 2018; 6(3): 370–381.BabuRVan DykeDLBhattacharyaSDevVGLiuMKwonMA rapid and reliable chromosome analysis method for products of conception using interphase nucleiMol Genet Genomic Med201863370381Search in Google Scholar
Pylyp LY, Spynenko LO, Verhoglyad NV, Mishenko AO, Mykytenko DO, Zukin VD. Chromosomal abnormalities in products of conception of first-trimester miscarriages detected by conventional cytogenetic analysis: a review of 1000 cases. J Assist Reprod Genet. 2018; 35(2): 265–271.PylypLYSpynenkoLOVerhoglyadNVMishenkoAOMykytenkoDOZukinVDChromosomal abnormalities in products of conception of first-trimester miscarriages detected by conventional cytogenetic analysis: a review of 1000 casesJ Assist Reprod Genet2018352265271Search in Google Scholar
Turki RF, Assidi M, Banni HA, Zahed HA, Karim S, Schulten H, et al. Associations of recurrent miscarriages with chromosomal abnormalities, thrombophilia allelic polymorphisms and/or consanguinity in Saudi Arabia. BMC Med Genet. 2016; 17(Suppl 1): 69.TurkiRFAssidiMBanniHAZahedHAKarimSSchultenHAssociations of recurrent miscarriages with chromosomal abnormalities, thrombophilia allelic polymorphisms and/or consanguinity in Saudi ArabiaBMC Med Genet201617Suppl 169Search in Google Scholar
Shen J, Wu W, Gao C, Ochin H, Qu D, Xie J, et al. Chromosomal copy number analysis on chorionic villus samples from early spontaneous miscarriages by high throughput genetic technology. Mol Cytogenet. 2016; 9: 7.ShenJWuWGaoCOchinHQuDXieJChromosomal copy number analysis on chorionic villus samples from early spontaneous miscarriages by high throughput genetic technologyMol Cytogenet201697Search in Google Scholar
Gug C, Burada F, Ioana M, Riza AL, Moldovan M, Mozos I, et al. Polyploidy in First and Second Trimester Pregnancies in Romania - a Retrospective Study. Clin Lab. 2020; 66(4). doi: 10.7754/Clin.Lab.2019.190649GugCBuradaFIoanaMRizaALMoldovanMMozosIPolyploidy in First and Second Trimester Pregnancies in Romania - a Retrospective StudyClin Lab202066410.7754/Clin.Lab.2019.190649Open DOISearch in Google Scholar
Russo R, Sessa AM, Fumo R, Gaeta S. Chromosomal anomalies in early spontaneous abortions: interphase FISH analysis on 855 FFPE first trimester abortions. Prenat Diagn. 2016; 36(2): 186–191.RussoRSessaAMFumoRGaetaSChromosomal anomalies in early spontaneous abortions: interphase FISH analysis on 855 FFPE first trimester abortionsPrenat Diagn2016362186191Search in Google Scholar
Brancati F, Mingarelli R, Dallapiccola B. Recurrent triploidy of maternal origin. Eur J Hum Genet. 2003; 11(12): 972–974.BrancatiFMingarelliRDallapiccolaBRecurrent triploidy of maternal originEur J Hum Genet20031112972974Search in Google Scholar
Carson JC, Hoffner L, Conlin L, Parks WT, Fisher RA, Spinner N, et al. Diploid/triploid mixoploidy: A consequence of asymmetric zygotic segregation of parental genomes. Am J Med Genet A. 2018; 176(12): 2720–2732.CarsonJCHoffnerLConlinLParksWTFisherRASpinnerNDiploid/triploid mixoploidy: A consequence of asymmetric zygotic segregation of parental genomesAm J Med Genet A20181761227202732Search in Google Scholar
Kolarski M, Ahmetovic B, Beres M, Topic R, Nikic V, Kavecan I, et al. Genetic Counseling and Prenatal Diagnosis of Triploidy During the Second Trimester of Pregnancy. Med Arch. 2017; 71(2): 144–147.KolarskiMAhmetovicBBeresMTopicRNikicVKavecanIGenetic Counseling and Prenatal Diagnosis of Triploidy During the Second Trimester of PregnancyMed Arch2017712144147Search in Google Scholar
Dória S, Lima V, Carvalho B, Moreira ML, Sousa M, Barros A, et al. Application of touch FISH in the study of mosaic tetraploidy and maternal cell contamination in pregnancy losses. J Assist Reprod Genet. 2010; 27(11): 657–662.DóriaSLimaVCarvalhoBMoreiraMLSousaMBarrosAApplication of touch FISH in the study of mosaic tetraploidy and maternal cell contamination in pregnancy lossesJ Assist Reprod Genet20102711657662Search in Google Scholar
Soler A, Badenas C, Margarit E, Madrigal I, Muñoz M, Borobio V, et al. A 92, XXXY Miscarriage Consecutive to a Digynic Triploid Pregnancy. Cytogenet Genome Res. 2016; 149(4): 258–261.SolerABadenasCMargaritEMadrigalIMuñozMBorobioVA 92, XXXY Miscarriage Consecutive to a Digynic Triploid PregnancyCytogenet Genome Res20161494258261Search in Google Scholar
Stefanova I, Jenderny J, Kaminsky E, Mannhardt A, Meinecke P, Grozdanova L, et al. Mosaic and complete tetraploidy in live-born infants: two new patients and review of the literature. Clin Dysmorphol. 2010; 19(3): 123–127.StefanovaIJendernyJKaminskyEMannhardtAMeineckePGrozdanovaLMosaic and complete tetraploidy in live-born infants: two new patients and review of the literatureClin Dysmorphol2010193123127Search in Google Scholar
Lee JM, Shin SY, Kim GW, Kim WJ, Wie JH, Hong S, et al. Optimizing the Diagnostic Strategy to Identify Genetic Abnormalities in Miscarriage. Mol Diagn Ther. 2021; 25(3): 351–359.LeeJMShinSYKimGWKimWJWieJHHongSOptimizing the Diagnostic Strategy to Identify Genetic Abnormalities in MiscarriageMol Diagn Ther2021253351359Search in Google Scholar
Gug C, Rațiu A, Navolan D, Drăgan I, Groza IM, Păpurică M, et al. Incidence and Spectrum of Chromosome Abnormalities in Miscarriage Samples: A Retrospective Study of 330 Cases. Cytogenet Genome Res. 2019; 158(4): 171–183.GugCRațiuANavolanDDrăganIGrozaIMPăpuricăMIncidence and Spectrum of Chromosome Abnormalities in Miscarriage Samples: A Retrospective Study of 330 CasesCytogenet Genome Res20191584171183Search in Google Scholar
Lathi RB, Gray Hazard FK, Heerema-McKenney A, Taylor J, Chueh JT. First trimester miscarriage evaluation. Semin Reprod Med. 2011; 29(6): 463–9.LathiRBGray HazardFKHeerema-McKenneyATaylorJChuehJTFirst trimester miscarriage evaluationSemin Reprod Med20112964639Search in Google Scholar
Oliveira AF, Torrão MM, Nogueira R, Ferreira M. Recurrent fetal triploidy: is there a genetic cause? BMJ Case Rep. 2021; 14(3): e239843.OliveiraAFTorrãoMMNogueiraRFerreiraMRecurrent fetal triploidy: is there a genetic cause?BMJ Case Rep2021143e239843Search in Google Scholar
Xu Q, Chan Y, Feng Y, Zhu B, Yang B, Zhu S, et al. Factors associated with fetal karyotype in spontaneous abortion: a case-case study. BMC Pregnancy Childbirth. 2022; 22(1): 320. doi: 10.1186/s12884-022-04491-8.XuQChanYFengYZhuBYangBZhuSFactors associated with fetal karyotype in spontaneous abortion: a case-case studyBMC Pregnancy Childbirth202222132010.1186/s12884-022-04491-8Open DOISearch in Google Scholar
Massalska D, Ozdarska K, Roszkowski T, Bijok J, Kucińska-Chahwan A, Panek GM, et al. Distribution of diandric and digynic triploidy depending on gestational age. J Assist Reprod Genet. 2021; 38(9): 2391–2395.MassalskaDOzdarskaKRoszkowskiTBijokJKucińska-ChahwanAPanekGMDistribution of diandric and digynic triploidy depending on gestational ageJ Assist Reprod Genet202138923912395Search in Google Scholar
Zaragoza MV, Surti U, Redline RW, Millie E, Chakravarti A, Hassold TJ. Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole. Am J Hum Genet. 2000; 66(6): 1807–20.ZaragozaMVSurtiURedlineRWMillieEChakravartiAHassoldTJParental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform moleAm J Hum Genet2000666180720Search in Google Scholar
Wiener-Megnazi Z, Auslender R, Dirnfeld M. Advanced paternal age and reproductive outcome. Asian J Androl. 2012; 14(1): 69–76.Wiener-MegnaziZAuslenderRDirnfeldMAdvanced paternal age and reproductive outcomeAsian J Androl20121416976Search in Google Scholar