BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

111 related articles for article (PubMed ID: 10465114)

  • 1. Simultaneous occurrence of two supernumerary autosomal ring chromosomes r(1) and r(16) in twins.
    Shanske AL; Dowling P; Schmidt R; White BJ; Russell B; Bogdanow A; Marion RW
    J Med Genet; 1999 Aug; 36(8):625-8. PubMed ID: 10465114
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
    In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Meiotic origin of two ring chromosomes 18 in a girl with developmental delay.
    Baumer A; Giovannucci Uzielli ML; Guarducci S; Lapi E; Röthlisberger B; Schinzel A
    Am J Med Genet; 2002 Nov; 113(1):101-4. PubMed ID: 12400074
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. "Ring syndrome" involving chromosome 2 confirmed by FISH analysis using chromosome-specific subtelomeric probes.
    Kosho T; Matsushima K; Sahashi T; Mitsui N; Fukushima Y; Sobajima H; Ohashi H
    Genet Couns; 2005; 16(1):65-70. PubMed ID: 15844781
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Five cases of supernumerary small ring chromosomes 1: heterogeneity and genotype-phenotype correlation.
    Bernardini L; Capalbo A; D'Avanzo MG; Torrente I; Grammatico P; Dell'Edera D; Cavalcanti DP; Novelli A; Dallapiccola B
    Eur J Med Genet; 2007; 50(2):94-102. PubMed ID: 17236832
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Identification and characterization of marker chromosome in Turner syndrome].
    Tan YQ; Cheng DH; DI YF; Li LY; Lu GX
    Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Supernumerary ring chromosome in a Bednar tumor (pigmented dermatofibrosarcoma protuberans) is composed of interspersed sequences from chromosomes 17 and 22: a fluorescence in situ hybridization and comparative genomic hybridization analysis.
    Nishio J; Iwasaki H; Ishiguro M; Ohjimi Y; Yo S; Isayama T; Naito M; Kikuchi M
    Genes Chromosomes Cancer; 2001 Mar; 30(3):305-9. PubMed ID: 11170290
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
    Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
    Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of a de novo 48,XX,+r(X),+r(17) by in situ hybridization in a patient with neurofibromatosis (NF1).
    Wiktor A; Van Dyke DL; Weiss L
    Am J Med Genet; 1993 Jan; 45(1):22-4. PubMed ID: 8418653
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Malignant refractory epilepsy in identical twins mosaic for a supernumerary ring chromosome 19.
    Shahwan A; Green AJ; Carey A; Stallings RL; O'Flaherty OC; King MD
    Epilepsia; 2004 Aug; 45(8):997-1000. PubMed ID: 15270770
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A boy with small supernumerary marker chromosome X identified by FISH.
    Koç A; Yirmibeş Karaoğuz M; Pala E; Kan D; Karaer K; Gücüyener K; Perçin EF
    Genet Couns; 2007; 18(4):393-9. PubMed ID: 18286820
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular cytogenetic characterization of ring chromosome 4 in a female having a chromosomally normal child.
    Lee MH; Park SY; Kim YM; Kim JM; Yoo KJ; Lee HH; Ryu HM
    Cytogenet Genome Res; 2005; 111(2):175-8. PubMed ID: 16103661
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping.
    Peschka B; Leygraaf J; Hansmann D; Hansmann M; Schröck E; Ried T; Engels H; Schwanitz G; Schubert R
    Prenat Diagn; 1999 Dec; 19(12):1143-9. PubMed ID: 10590433
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of supernumerary der(20) chromosomes by FISH in three patients.
    Viersbach R; Engels H; Schwanitz G
    Am J Med Genet; 1997 Jun; 70(3):278-83. PubMed ID: 9188666
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
    Chantot-Bastaraud S; Muti C; Pipiras E; Routon MC; Roubergue A; Burglen L; Siffroi JP; Simon-Bouy B
    Ann Genet; 2004; 47(3):241-9. PubMed ID: 15337469
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cytogenetic and molecular analysis of a ring (21) in a patient with partial trisomy 21 and megakaryocytic leukemia.
    Palmer CG; Blouin JL; Bull MJ; Breitfeld P; Vance GH; Van Meter T; Weaver DD; Heerema NA; Colbern SG; Korenberg JR
    Am J Med Genet; 1995 Jul; 57(4):527-36. PubMed ID: 7573123
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.