Complex small supernumerary marker chromosomes - An update

Molecular Cytogenetics

Volumn 6, Issue 1, 2013, Pages

  Liehr, Thomas ^a,l   Cirkovic, Sanja ^b   Lalic, Tanja ^b   Guc Scekic, Marija ^b,c   De Almeida, Cynthia ^d   Weimer, Jörg ^e   Iourov, Ivan ^f,g   Melaragno, Maria Isabel ^h   Guilherme, Roberta S ^h   Stefanou, Eunice Georgia G ⁱ   Aktas, Dilek ^j   Kreskowski, Katharina ^a   Klein, Elisabeth ^a   Ziegler, Monika ^a   Kosyakova, Nadezda ^a   Volleth, Marianne ^k   Hamid, Ahmed B ^a  

^a JENA UNIVERSITY HOSPITAL   (Germany)

^b Mother and Child Health Care Institute of Serbia Dr Vukan Cupic   (Serbia)

^c UNIVERSITY OF BELGRADE   (Serbia)

^d UNIVERSIDAD DE LA REPÚBLICA   (Uruguay)

^e UKSH Campus Kiel ^*  (Germany)

^f MENTAL HEALTH RESEARCH CENTER   (Russian Federation)

^g N N BLOKHIN NATIONAL MEDICAL RESEARCH CENTER OF ONCOLOGY   (Russian Federation)

^h FEDERAL UNIVERSITY OF SÃO PAULO   (Brazil)

ⁱ UNIVERSITY GENERAL HOSPITAL OF PATRAS   (Greece)

^j HACETTEPE UNIVERSITY   (Turkey)

^k UNIVERSITY HOSPITAL MAGDEBURG   (Germany)

^l Postfach   (Germany)

more..

Author keywords

Complex small supernumerary marker chromosomes (sSMC); Emanuel syndrome; Genotype phenotype correlation; Mosaicism; SSMC shape

Indexed keywords

ACROCENTRIC CHROMOSOME; ARTICLE; CHROMOSOME 10; CHROMOSOME BREAKAGE; CHROMOSOME DISORDER; CHROMOSOME STRUCTURE; FEMALE; HUMAN; KARYOTYPE; MAJOR CLINICAL STUDY; MALE; MOSAICISM; PRIORITY JOURNAL; SUPERNUMERARY MARKER CHROMOSOME;

EID: 84886739186     PISSN: None     EISSN: 17558166     Source Type: Journal    
DOI: 10.1186/1755-8166-6-46     Document Type: Article

References (8)

1. Small supernumerary marker chromosomes (sSMC) in humans. Liehr T, Claussen U, Starke H, Cytogenet Genome Res 2004 107 55 67 10.1159/000079572 15305057 (Pubitemid 39140346)
2. Liehr T, Small Supernumerary Marker Chromosomes (sSMC) A Guide for Human Geneticists and Clinicians; With contributions by UNIQUE (The Rare Chromosome Disorder Support Group) Heidelberg, Dordrecht, London, New York: Springer 2012
3. Liehr T, Small supernumerary marker chromosomes http://www.fish. uniklinikum-jena.de/sSMC.html. [accessed 23/09/2013
4. Neocentric small supernumerary marker chromosomes (sSMC)-three more cases and review of the literature. Liehr T, Utine GE, Trautmann U, Rauch A, Kuechler A, Pietrzak J, Bocian E, Kosyakova N, Mrasek K, Boduroglu K, Weise A, Aktas D, Cytogenet Genome Res 2007 118 31 37 10.1159/000106438 17901697 (Pubitemid 47492009)
5. Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity? 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, Mol Cytogenet 2008 1 6 10.1186/1755-8166-1-6 18471318
6. A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21). Sheridan MB, Kato T, Haldeman-Englert C, Jalali GR, Milunsky JM, Zou Y, Klaes R, Gimelli G, Gimelli S, Gemmill RM, Drabkin HA, Hacker AM, Brown J, Tomkins D, Shaikh TH, Kurahashi H, Zackai EH, Emanuel BS, Am J Hum Genet 2010 87 209 218 10.1016/j.ajhg.2010.07. 002 20673865
7. The t(4;8) is mediated by homologous recombination between olfactory receptor gene clusters, but other 4p16 translocations occur at random. Maas NM, Van Vooren S, Hannes F, Van Buggenhout G, Mysliwiec M, Moreau Y, Fagan K, Midro A, Engiz O, Balci S, Parker MJ, Sznajer Y, Devriendt K, Fryns JP, Vermeesch JR, Genet Couns 2007 18 357 365 18286816
8. Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements. Liehr T, Kosayakova N, Schröder J, Ziegler M, Kreskowski K, Pohle B, Bhatt S, Theuss L, Wilhelm K, Weise A, Mrasek K, Balk J Med Genet 2011 14 13 16