BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

248 related articles for article (PubMed ID: 17901697)

  • 1. 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(1):31-7. PubMed ID: 17901697
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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. PubMed ID: 18391547
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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. PubMed ID: 20017317
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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. PubMed ID: 18506363
    [TBL] [Abstract][Full Text] [Related]  

  • 5. New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank.
    Tönnies H; Pietrzak J; Bocian E; MacDermont K; Kuechler A; Belitz B; Trautmann U; Schmidt A; Schulze B; Rodríguez L; Binkert F; Yardin C; Kosyakova N; Volleth M; Mkrtchyan H; Schreyer I; von Eggeling F; Weise A; Mrasek K; Liehr T
    J Histochem Cytochem; 2007 Jun; 55(6):651-60. PubMed ID: 17341473
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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. PubMed ID: 16915592
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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. PubMed ID: 19729913
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitotic stability of small supernumerary marker chromosomes: a study based on 93 immortalized cell lines.
    Spittel H; Kubek F; Kreskowski K; Ziegler M; Klein E; Hamid AB; Kosyakova N; Radhakrishnan G; Junge A; Kozlowski P; Schulze B; Martin T; Huhle D; Mehnert K; Rodríguez L; Ergun MA; Sarri C; Militaru M; Stipoljev F; Tittelbach H; Vasheghani F; de Bello Cioffi M; Hussein SS; Fan X; Volleth M; Liehr T
    Cytogenet Genome Res; 2014; 142(3):151-60. PubMed ID: 24714101
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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. PubMed ID: 17546703
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A neocentric isochromosome Yp present as additional small supernumerary marker chromosome--evidence against U-type exchange mechanism?
    Sheth F; Ewers E; Kosyakova N; Weise A; Sheth J; Patil S; Ziegler M; Liehr T
    Cytogenet Genome Res; 2009; 125(2):115-6. PubMed ID: 19729914
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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. PubMed ID: 15750022
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?
    Guilherme RS; Klein E; Venner C; Hamid AB; Bhatt S; Melaragno MI; Volleth M; Polityko A; Kulpanovich A; Kosyakova N; Liehr T
    Chromosome Res; 2012 Oct; 20(7):825-35. PubMed ID: 23076733
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Is there a yet unreported unbalanced chromosomal abnormality without phenotypic consequences in proximal 4p?
    Liehr T; Bartels I; Zoll B; Ewers E; Mrasek K; Kosyakova N; Merkas M; Hamid AB; von Eggeling F; Posorski N; Weise A
    Cytogenet Genome Res; 2011; 132(1-2):121-3. PubMed ID: 20639618
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics.
    Liehr T; Weise A
    Int J Mol Med; 2007 May; 19(5):719-31. PubMed ID: 17390076
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21 -->13q22 chromosome and balancing reciprocal deletion.
    Knegt AC; Li S; Engelen JJ; Bijlsma EK; Warburton PE
    Prenat Diagn; 2003 Mar; 23(3):215-20. PubMed ID: 12627422
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Five novel locations of Neocentromeres in human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and heterochromatin of unknown origin.
    Klein E; Rocchi M; Ovens-Raeder A; Kosyakova N; Weise A; Ziegler M; Meins M; Morlot S; Fischer W; Volleth M; Polityko A; Ogilvie CM; Kraus C; Liehr T
    Cytogenet Genome Res; 2012; 136(3):163-6. PubMed ID: 22377933
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Small supernumerary marker chromosomes (sSMC) in humans.
    Liehr T; Claussen U; Starke H
    Cytogenet Genome Res; 2004; 107(1-2):55-67. PubMed ID: 15305057
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics.
    Liehr T
    Methods Mol Biol; 2008; 444():27-38. PubMed ID: 18425469
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences.
    Liehr T; Stumm M; Wegner RD; Bhatt S; Hickmann P; Patsalis PC; Meins M; Morlot S; Klaschka V; Ewers E; Hinreiner S; Mrasek K; Kosyakova N; Cai WW; Cheung SW; Weise A
    Cytogenet Genome Res; 2009; 124(1):102-5. PubMed ID: 19372675
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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. PubMed ID: 19435454
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.