References
- Liehr T, Claussen U, Starke H. Small supernumerary marker chromosomes (sSMC) in humans. Cytogenet Genome Res 2004;107:55–67.
- Liehr T, Weise A. Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics. Int J Mol Med 2007;19:719–731.
- Liehr T, Karamysheva T, Merkas M, Brecevic L, Hamid AB, Ewers E, Mrasek K, et al. Somatic mosaicism in cases with small supernumerary marker chromosomes. Curr Genomics 2010;11:432–439.
- Liehr T, Mrasek K, Weise A, Dufke A, Rodríguez L, Martínez Guardia N, Sanchís A, et al. Small supernumerary marker chromosomes–progress towards a genotype-phenotype correlation. Cytogenet Genome Res 2006;112:23–34.
- Srebniak MI, Boter M, Oudesluijs GO, Cohen-Overbeek T, Govaerts LC, Diderich KE, Oegema R, et al. Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities. Mol Cytogenet 2012;5:14.
- Liehr T, Wegner RD, Stumm M, Joksic G, Polityko A, Kosyakova N, Ewers E, et al. Pallister-Killian syndrome. Rare phenotypic features and variable karyotypes. Balkan J Med Genet 2008;12:65–67.
- Footz TK, Brinkman-Mills P, Banting GS, Maier SA, Riazi MA, Bridgland L, Hu S, et al. Analysis of the cat eye syndrome critical region in humans and the region of conserved synteny in mice: a search for candidate genes at or near the human chromosome 22 pericentromere. Genome Res 2001;11:1053–1070.
- Balkan M, Isi H, Gedik A, Erdemoglu M, Budak T. A small supernumerary marker chromosome, derived from chromosome 22, possibly associated with repeated spontaneous abortions. Genet Mol Res 2010;9:1683–1689.
- Manvelyan M, Riegel M, Santos M, Fuster C, Pellestor F, Mazaurik ML, Schulze B, et al. Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature. Int J Mol Med 2008;21:705–714.
- Paetzold U, Schwanitz G, Schubert R, van der Ven K, Montag M. Sperm analyses, genetic counselling and therapy in an infertile carrier of a supernumerary marker chromosome 15. Adv Med Sci 2006;51:31–35.
- Sheth F, Ewers E, Kosyakova N, Weise A, Sheth J, Patil S, Ziegler M, Liehr T. A neocentric isochromosome Yp present as additional small supernumerary marker chromosome–evidence against U-type exchange mechanism? Cytogenet Genome Res 2009;125:115–116.
- Murmann AE, Conrad DF, Mashek H, Curtis CA, Nicolae RI, Ober C, Schwartz S. Inverted duplications on acentric markers: mechanism of formation. Hum Mol Genet 2009;18:2241–2256.
- Liehr T, Ewers E, Hamid AB, Kosyakova N, Voigt M, Weise A, Manvelyan M. Small supernumerary marker chromosomes and uniparental disomy have a story to tell. J Histochem Cytochem 2011;59:842–848.
- Liehr T, Stumm M, Wegner RD, Bhatt S, Hickmann P, Patsalis PC, Meins M, et al. 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences. Cytogenet Genome Res 2009;124:102–105.
- Baldwin EL, May LF, Justice AN, Martin CL, Ledbetter DH. Mechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues. Am J Hum Genet 2008;82:398–410.
- Inaba Y, Wong LH, Choo KHA. Development of Neocentromere-based minichromosome gene delivery system ASHG 2010, abstract 3074.
- Pérez-Luz S, Díaz-Nido J. Prospects for the use of artificial chromosomes and minichromosome-like episomes in gene therapy. J Biomed Biotechnol 2010;2010.
- Raimondi E. Naturally occurring minichromosome platforms in chromosome engineering: an overview. Methods Mol Biol 2011;738:41–56.