PubMed

A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1-q12.1 in a healthy man.

Rodríguez L, Liehr T, Martínez-Fernández ML, Lara A, Torres A, Martínez-Frías ML.

Mol Cytogenet. 2008 Apr 2;1:4.PMID: 18471313 [PubMed - in process]Related articlesFree article

Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.

Melo JB, Matoso E, Polityko A, Saraiva J, Backx L, Vermeesch JR, Kosyakova N, Ewers E, Liehr T, Carreira IM.

Cytogenet Genome Res. 2009;125(2):109-14. Epub 2009 Aug 31.PMID: 19729913 [PubMed - indexed for MEDLINE]Related articles

Familial small supernumerary marker chromosome (sSMC) (14)(:P11-q11:)In a child with translocation down syndrome.

Vundinti BR, Korgaonkar S, Ghosh K.

Indian J Pediatr. 2009 Dec;76(12):1265-7. Epub 2009 Dec 11.PMID: 20012787 [PubMed - in process]Related articles

Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients.

Pietrzak J, Mrasek K, Obersztyn E, Stankiewicz P, Kosyakova N, Weise A, Cheung SW, Cai WW, von Eggeling F, Mazurczak T, Bocian E, Liehr T.

J Appl Genet. 2007;48(2):167-75.PMID: 17495351 [PubMed - indexed for MEDLINE]Related articlesFree article

Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.

Liehr T, Starke H, Senger G, Melotte C, Weise A, Vermeesch JR.

Am J Med Genet A. 2006 Jan 1;140(1):46-51. Review.PMID: 16333826 [PubMed - indexed for MEDLINE]Related articles

Another small supernumerary marker chromosome (sSMC) derived from chromosome 2: towards a genotype/phenotype correlation.

Mrasek K, Starke H, Liehr T.

J Histochem Cytochem. 2005 Mar;53(3):367-70.PMID: 15750022 [PubMed - indexed for MEDLINE]Related articlesFree article

Small supernumerary chromosome marker generating complete and pure trisomy 18p, characterized by molecular cytogenetic techniques and review.

Rodríguez L, Liehr T, Mrasek K, Mansilla E, Martínez-Fernández ML, Garcia A, Martínez-Frías ML.

Am J Med Genet A. 2007 Nov 15;143A(22):2727-32. Review.PMID: 17937429 [PubMed - indexed for MEDLINE]Related articles

Molecular cytogenetic characterization of two small chromosome 8 derived supernumerary mosaic markers.

Herry A, Morel F, Le Bris MJ, Bellec V, Lallaoui H, Parent P, De Braekeleer M.

Am J Med Genet A. 2004 Jul 1;128A(1):33-8.PMID: 15211653 [PubMed - indexed for MEDLINE]Related articles

First small supernumerary ring chromosome carrying 10q euchromatin in a patient with mild phenotype characterized by molecular cytogenetic techniques and review of the literature.

Trimborn M, Grueters A, Neitzel H, Tönnies H.

Cytogenet Genome Res. 2005;108(4):278-82. Review.PMID: 15627745 [PubMed - indexed for MEDLINE]Related articles

Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines.

Brecevic L, Michel S, Starke H, Müller K, Kosyakova N, Mrasek K, Weise A, Liehr T.

Cytogenet Genome Res. 2006;114(3-4):319-24.PMID: 16954673 [PubMed - indexed for MEDLINE]Related articles

Severe psychomotor retardation in a boy with a small supernumerary marker chromosome 19p.

Vraneković J, Brajenović-Milić B, Modrusan-Mozetić Z, Babić I, Kapović M.

Cytogenet Genome Res. 2008;121(3-4):298-301. Epub 2008 Aug 29.PMID: 18758176 [PubMed - indexed for MEDLINE]Related articles

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male.

Kitsiou-Tzeli S, Manolakos E, Lagou M, Kontodiou M, Kosyakova N, Ewers E, Weise A, Garas A, Orru S, Liehr T, Metaxotou A.

Mol Cytogenet. 2009 Jan 7;2:1.PMID: 19128450 [PubMed - in process]Related articlesFree article

Mosaic trisomy (8)(p22 --> pter) in a fetus caused by a supernumerary marker chromosome without alphoid sequences.

de Pater JM, Kroes HY, Verschuren M, van Oppen AC, Albrechts JC, Engelen JJ.

Prenat Diagn. 2005 Feb;25(2):151-5.PMID: 15712342 [PubMed - indexed for MEDLINE]Related articles

Characterization of a familial small supernumerary marker chromosome in a patient with adult-onset tongue cancer.

Bakshi SR, Dave BJ, Sanger W, Brahmbhatt MM, Trivedi PJ, Kakadia PM, Patel SJ.

Cytogenet Genome Res. 2008;121(1):14-7. Epub 2008 May 7.PMID: 18544921 [PubMed - indexed for MEDLINE]Related articles

Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient.

Liehr T, Mrasek K, Starke H, Claussen U, Schreiber G.

Cytogenet Genome Res. 2005;111(2):179-81.PMID: 16103662 [PubMed - indexed for MEDLINE]Related articles

Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literature.

Liehr T, Mrasek K, Hinreiner S, Reich D, Ewers E, Bartels I, Seidel J, Emmanuil N, Petesen M, Polityko A, Dufke A, Iourov I, Trifonov V, Vermeesch J, Weise A.

Sex Dev. 2007;1(6):353-62. Epub 2008 Jan 18. Review.PMID: 18391547 [PubMed - indexed for MEDLINE]Related articles

Analphoid supernumerary marker chromosome characterized by aCGH and FISH as inv dup(3)(q25.33qter) de novo in a child with dysmorphic features and streaky pigmentation: case report.

Murthy SK, Malhotra AK, Jacob PS, Naveed S, Al-Rowaished EE, Mani S, Padariyakam S, Pramathan R, Nath R, Al-Ali MT, Al-Gazali L.

Mol Cytogenet. 2008 Aug 14;1:19.PMID: 18700989 [PubMed - in process]Related articlesFree article

Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature.

Manvelyan M, Riegel M, Santos M, Fuster C, Pellestor F, Mazaurik ML, Schulze B, Polityko A, Tittelbach H, Reising-Ackermann G, Belitz B, Hehr U, Kelbova C, Volleth M, Gödde E, Anderson J, Küpferling P, Köhler S, Duba HC, Dufke A, Aktas D, Martin T, Schreyer I, Ewers E, Reich D, Mrasek K, Weise A, Liehr T.

Int J Mol Med. 2008 Jun;21(6):705-14.PMID: 18506363 [PubMed - indexed for MEDLINE]Related articles

A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1--evidence for high variability in mosaicism in different tissues of sSMC carriers.

Fickelscher I, Starke H, Schulze E, Ernst G, Kosyakova N, Mkrtchyan H, MacDermont K, Sebire N, Liehr T.

Prenat Diagn. 2007 Aug;27(8):783-5.PMID: 17546703 [PubMed - indexed for MEDLINE]Related articles

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 Apr 15;1:6.PMID: 18471318 [PubMed - in process]Related articlesFree article