https://orcid.org/0000-0003-2672-0439
References
- de Ravel TJ, Vermeesch JR, Fryns JP. De novo interstitial tandem duplication of chromosome 20p12.1p13. Am J Med Genet A. 2003;117A(1):76–79. doi:10.1002/ajmg.a.10825
- Bartolini L, Sartori S, Lenzini E, et al. De novo trisomy 20p characterized by array comparative genomic hybridization: report of a novel case and review of the literature. Gene. 2013;524(2):368–372. doi:10.1016/j.gene.2013.04.033
- Sidwell RU, Pinson MP, Gibbons B, et al. Pure trisomy 20p resulting from isochromosome formation and whole arm translocation. J Med Genet. 2000;37(6):454–458. doi:10.1136/jmg.37.6.454
- Grammatico P, Cupilari F, Di Rosa C, Falcolini M, Del Porto G. 20 p duplication as a result of parental translocation: familial case report and a contribution to the clinical delineation of the syndrome. Clin Genet. 1992;41(6):285–289. doi:10.1111/j.1399-0004.1992.tb03398.x
- Grimbizis GF, Gordts S, Di Spiezio Sardo A, et al. The ESHRE/ESGE consensus on the classification of female genital tract congenital anomalies. Hum Reprod. 2013;28(8):2032–2044. doi:10.1093/humrep/det098
- Reyes-Muñoz E, Vitale SG, Alvarado-Rosales D, et al. Müllerian anomalies prevalence diagnosed by hysteroscopy and laparoscopy in mexican infertile women: results from a cohort study. Diagnostics (Basel). 2019;9:4.
- Choi J, Yoon SY, Park BG, Eun BL, Kim M, Kwon JA. De novo pure trisomy 20p: report of a novel case of a marker chromosome and literature review. Ann Lab Med. 2020;40(3):277–280. doi:10.3343/alm.2020.40.3.277
- Oppenheimer S, Dignan P, Soukup S. Partial trisomy 20p: familial occurrence. Am J Med Genet. 2000;95(4):316–319. doi:10.1002/1096-8628(20001211)95:4<316::AID-AJMG4>3.0.CO;2-Z
- Wieczorek D, Bartsch O, Gillessen-Kaesbach G. Distal monosomy 18p/distal trisomy 20p–a recognizable facial phenotype? Am J Med Genet A. 2003;120A(3):429–433. doi:10.1002/ajmg.a.20060
- Molina-Gomes D, Nebout V, Daikha-Dahmane F, Vialard F, Ville Y, Selva J. Partial trisomy 20p resulting from recombination of a maternal pericentric inversion: case report of a prenatal diagnosis by chorionic villus sampling. Prenat Diagn. 2006;26(3):239–241. doi:10.1002/pd.1389
- Leclercq S, Maincent K, Baverel F, et al. Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U-type exchange model. Am J Med Genet A. 2009;149A(3 Mar):437–445. doi:10.1002/ajmg.a.32640
- Lin PC, Bhatnagar KP, Nettleton GS, Nakajima ST. Female genital anomalies affecting reproduction. Fertil Steril. 2002;78(5):899–915. doi:10.1016/S0015-0282(02)03368-X
- Bhagavath B, Ellie G, Griffiths KM, et al. Uterine malformations: an update of diagnosis, management, and outcomes. Obstet Gynecol Surv. 2017;72(6):377–392. doi:10.1097/OGX.0000000000000444
- Oppelt P, von Have M, Paulsen M, et al. Female genital malformations and their associated abnormalities. Fertil Steril. 2007;87(2):335–342. doi:10.1016/j.fertnstert.2006.07.1501