[Wiseman FK, Alford KA, Tybulewicz VL, Fisher EM. Down syndrome-recent progress and future prospects. Hum Mol Genet 2009; 18(R1): R75-R83.10.1093/hmg/ddp010265794319297404]Search in Google Scholar
[Hultén MA, Patel SD, Tankimanova M, Westgren M, Papadogiannakis N, Jonsson AM, Iwarsson E. On the origin of trisomy 21 Down syndrome. Mol Cytogenet 2008; 1: 21.10.1186/1755-8166-1-21256495718801168]Search in Google Scholar
[Migliore L, Migheli F, Coppedè F. Susceptibility to aneuploidy in young mothers of Down syndrome children. TheScientificWorldJournal 2009; 9: 1052-1060 (see http://thescientificworld.co.uk/headeradmin/upload/2009.06.122.pdf). http://thescientificworld.co.uk/headeradmin/upload/2009.06.122.pdf10.1100/tsw.2009.122582314519802501]Search in Google Scholar
[Liehr T, Claussen U, Starke H. Small supernumerary marker chromosomes (sSMC) in humans. Cytogenet Genome Res 2004; 107(1-2): 55-67.10.1159/00007957215305057]Search in Google Scholar
[Liehr T. Small supernumerary marker chromosome homepage. http://www.med.uni-jena.de/fish/sSMC/00START.htm]Search in Google Scholar
[Trifonov V, Fluri S, Binkert F, Nandini A, Anderson J, Rodriguez L, Gross M, Kosyakova N, Mkrtchyan H, Ewers E, Reich D, Weise A, Liehr T. Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity? Mol Cytogenet 2008; 1: 6.10.1186/1755-8166-1-6237588118471318]Search in Google Scholar
[Liehr T, Starke H, Weise A, Lehrer H, Claussen U. Multicolor FISH probe sets and their applications. Histol Histopathol 2004; 19(1): 229-237.]Search in Google Scholar
[Starke H, Nietzel A, Weise A, Heller A, Mrasek K, Belitz B, Kelbova C, Volleth M, Albrecht B, Mitulla B, Trappe R, Bartels I, Adolph S, Dufke A, Singer S, Stumm M, Wegner RD, Seidel J, Schmidt A, Kuechler A, Schreyer I, Claussen U, von Eggeling F, Liehr T. Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification. Hum Genet 2003; 114(1): 51-67.10.1007/s00439-003-1016-313680362]Search in Google Scholar
[Jeanty C, Turner C. Prenatal diagnosis of double aneuploidy, 48, XXY, +21, and review of the literature. J Ultrasound Med 2009; 28(5): 673-681.10.7863/jum.2009.28.5.67319389908]Search in Google Scholar
[Kovaleva NV, Mutton DE. Epidemiology of double aneuploidies involving chromosome 21 and the sex chromosomes. Am J Med Genet A 2005; 134A(1): 24-32.10.1002/ajmg.a.3030615704133]Search in Google Scholar
[Mabboux P, Brisset S, Aboura A, Pineau D, Koubi V, Joannidis S, Labrune P, Tachdjian G. Pure and complete trisomy 18p due to a supernumerary marker chromosome associated with moderate mental retardation. Am J Med Genet A 2007; 143A(7): 727-733.10.1002/ajmg.a.3163317330860]Search in Google Scholar
[Rodriguez L, Liehr T, Mrasek K, Mansilla E, Martinez-Fernandez ML, Garcia A, Martinez-Frias ML. Small supernumerary chromosome marker generating complete and pure trisomy 18p, characterized by molecular cytogenetic techniques and review. Am J Med Genet A 2007; 143A(22): 2727-2732.10.1002/ajmg.a.3200317937429]Search in Google Scholar
[Minelli E, Müller-Navia J, Mazzola D, Mny P, Bronz L, Uhr M. Characterization of a marker chromosome with FISH and microdissection in prenatal diagnosis. Ann Genet 2003; 46(1): 325.]Search in Google Scholar
[Mrasek K, Heller A, Rubtsov N, Trifonov V, Starke H, Claussen U, Liehr T. Detailed Hylobates lar karyotype defined by 25-color FISH and multicolor banding. Int J Mol Med 2003; 12(2): 139-146.10.3892/ijmm.12.2.139]Search in Google Scholar