BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

730 related articles for article (PubMed ID: 17451694)

  • 1. 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. PubMed ID: 17451694
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Ring chromosome 21 and reproductive pattern: a familial case and review of the literature.
    Bertini V; Valetto A; Uccelli A; Tarantino E; Simi P
    Fertil Steril; 2008 Nov; 90(5):2004.e1-5. PubMed ID: 18371955
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
    Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Wu PC; Chen WL; Chen LF; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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. PubMed ID: 17495351
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
    Chen CP; Chen M; Chern SR; Wu PS; Chang SP; Lee DJ; Chen YT; Chen LF; Su JW; Hwa-Ruey Hsieh A; Hwa-Jiun Hsieh A; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):411-7. PubMed ID: 23040927
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 49(3):207-14. PubMed ID: 16762822
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Identification of marker chromosomes in thirteen patients using FISH probing.
    Daniel A; Malafiej P; Preece K; Chia N; Nelson J; Smith M
    Am J Med Genet; 1994 Oct; 53(1):8-18. PubMed ID: 7802042
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
    Tan YQ; Di YF; Song YZ; Cheng DH; Li LY; Lu GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):392-6. PubMed ID: 17680527
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Diagnosis of sex chromosome abnormality by fluorescence in-situ hybridization].
    Huang Y; Sun X; Li Q
    Zhonghua Yi Xue Za Zhi; 1999 Feb; 79(2):106-8. PubMed ID: 11601014
    [TBL] [Abstract][Full Text] [Related]  

  • 13. M-FISH applications in clinical genetics.
    Cetin Z; Berker Karaüzüm S; Yakut S; Mihçi E; Baumer A; Wey E; Taçoy S; Bağci G; Lüleci G
    Genet Couns; 2005; 16(3):257-68. PubMed ID: 16259323
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Primary amenorrhea in a woman with a cryptic complex chromosome rearrangement involving the critical regions Xp11.2 and Xq24.
    Hernando C; Plaja A; Català V; Sarret E; Egozcue J; Fuster C
    Fertil Steril; 2004 Dec; 82(6):1666-71. PubMed ID: 15589876
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Turner mosaicism (45,X/46,XX) diagnosed in a young woman subsequent to low oocyte maturity and failed ICSI.
    Moore AK; Lynch K; Arny MJ; Grow DR
    Fertil Steril; 2008 Nov; 90(5):2012.e13-5. PubMed ID: 18554592
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 2():1. PubMed ID: 19128450
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Use of chromosome painting for marker chromosome identification in two children with congenital disorders.
    Doco-Fenzy M; Navrocki B; Cornillet P; Sabouraud P; Robillard P; Gruson N; Gaillard D; Adnet JJ
    Bull Assoc Anat (Nancy); 1994 Jun; 78(241):9-13. PubMed ID: 8086666
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new approach to chromosomal abnormalities in sperm from patients with oligoasthenoteratozoospermia: detection of double aneuploidy in addition to single aneuploidy and diploidy by five-color fluorescence in situ hybridization using one probe set.
    Durakbasi-Dursun HG; Zamani AG; Kutlu R; Görkemli H; Bahce M; Acar A
    Fertil Steril; 2008 Jun; 89(6):1709-17. PubMed ID: 18036525
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Identification of human small supernumerary marker chromosomes and discussion of its research value].
    Ou J; Wang W; Duan CY; Fu WY; Liu YL; Sun J; Zhong HL; Li H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):91-4. PubMed ID: 23450489
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization.
    Manolakos E; Kefalas K; Neroutsou R; Lagou M; Kosyakova N; Ewers E; Ziegler M; Weise A; Tsoplou P; Rapti SM; Papoulidis I; Anastasakis E; Garas A; Sotiriou S; Eleftheriades M; Peitsidis P; Malathrakis D; Thomaidis L; Kitsos G; Orru S; Liehr T; Petersen MB; Kitsiou-Tzeli S
    Mol Med Rep; 2010; 3(6):1015-22. PubMed ID: 21472348
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 37.