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    Results: 1 to 20 of 214

    1.

    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]Free PMC ArticleFree textRelated citations

    2.

    Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success.

    Santos M, Mrasek K, Rigola MA, Starke H, Liehr T, Fuster C.

    Fertil Steril. 2007 Oct;88(4):969.e11-7. Epub 2007 Apr 23.PMID: 17451694 [PubMed - indexed for MEDLINE]Related citations

    3.

    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]Free ArticleRelated citations

    4.

    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 citations

    5.

    Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.

    Lin CC, Hsieh YY, Wang CH, Li YC, Hsieh LJ, Lee CC, Tsai CH, Tsai FJ.

    Prenat Diagn. 2006 Oct;26(10):898-902.PMID: 16915592 [PubMed - indexed for MEDLINE]Related citations

    6.

    Identification, counselling, and outcome of two cases of prenatally diagnosed supernumerary small ring chromosomes.

    Michalski K, Rauer M, Williamson N, Perszyk A, Hoo JJ.

    Am J Med Genet. 1993 Apr 1;46(1):88-94.PMID: 8494036 [PubMed - indexed for MEDLINE]Related citations

    7.

    Small supernumerary marker chromosomes 1 with a normal phenotype.

    Liehr T, Wegner RD, Stumm M, Martin T, Gillessen-Kaesbach G, Kosyakova N, Ewers E, Hamid AB, von Eggeling F, Hentschel J, Ziegler M, Weise A.

    J Chin Med Assoc. 2010 Apr;73(4):205-7.PMID: 20457442 [PubMed - in process]Related citations

    8.

    A series of supernumerary small ring marker autosomes identified by FISH with chromosome probe arrays and literature review excluding chromosome 15.

    Daniel A, Malafiej P.

    Am J Med Genet A. 2003 Mar 15;117A(3):212-22. Review.PMID: 12599184 [PubMed - indexed for MEDLINE]Related citations

    9.
    10.

    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 citations

    11.

    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]Free PMC ArticleFree textRelated citations

    12.

    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]Free ArticleRelated citations

    13.

    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 citations

    14.

    Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature.

    Chen CP, Lin CC, Li YC, Chern SR, Lee CC, Chen WL, Lee MS, Wang W, Tzen CY.

    Prenat Diagn. 2004 Oct;24(10):767-73. Review.PMID: 15503270 [PubMed - indexed for MEDLINE]Related citations

    15.

    [Analysis of the small supernumerary marker chromosome in Turner syndrome with 45, X/46, X, + mar karyotype]

    Ye ZC, Cai JG, Zhu XY, Zhao R, He XY, Zhong Y, Liu KX, Zhu YM.

    Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Aug;26(4):461-4. Chinese. PMID: 20017317 [PubMed - indexed for MEDLINE]Related citations

    16.

    Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face.

    Sarri C, Gyftodimou Y, Grigoriadou M, Pandelia E, Kalogirou S, Kokotas H, Mrasek K, Weise A, Petersen MB.

    Cytogenet Genome Res. 2006;114(3-4):330-7.PMID: 16954675 [PubMed - indexed for MEDLINE]Related citations

    17.

    Handling small supernumerary marker chromosomes in prenatal diagnostics.

    Liehr T, Ewers E, Kosyakova N, Klaschka V, Rietz F, Wagner R, Weise A.

    Expert Rev Mol Diagn. 2009 May;9(4):317-24. Review.PMID: 19435454 [PubMed - indexed for MEDLINE]Related citations

    18.

    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 citations

    19.

    The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey.

    Karaman B, Aytan M, Yilmaz K, Toksoy G, Onal EP, Ghanbari A, Engur A, Kayserili H, Yuksel-Apak M, Basaran S.

    Eur J Med Genet. 2006 May-Jun;49(3):207-14. Epub 2005 Jul 12.PMID: 16762822 [PubMed - indexed for MEDLINE]Related citations

    20.

    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 citations

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