BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

95 related articles for article (PubMed ID: 10340656)

  • 1. FISH characterization of two supernumerary r(1) associated with distinct clinical phenotypes.
    Giardino D; Bettio D; Gottardi G; Rizzi N; Pierluigi M; Perfumo C; Calì A; Dagna Bricarelli F; Larizza L
    Am J Med Genet; 1999 Jun; 84(4):377-80. PubMed ID: 10340656
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum.
    Li S; Malafiej P; Levy B; Mahmood R; Field M; Hughes T; Lockhart LH; Wu Z; Huang M; Hirschhorn K; Velagaleti GV; Daniel A; Warburton PE
    Am J Med Genet; 2002 Jul; 110(3):258-67. PubMed ID: 12116235
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Small familial supernumerary ring chromosome 2: FISH characterization and genotype-phenotype correlation.
    Giardino D; Finelli P; Russo S; Gottardi G; Rodeschini O; Atza MG; Natacci F; Larizza L
    Am J Med Genet; 2002 Aug; 111(3):319-23. PubMed ID: 12210331
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 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. Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses.
    Huang XL; de Michelena MI; Mark H; Harston R; Benke PJ; Price SJ; Milunsky A
    Clin Genet; 2005 Dec; 68(6):513-9. PubMed ID: 16283881
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Identification of an unusual marker chromosome by spectral karyotyping.
    Huang B; Ning Y; Lamb AN; Sandlin CJ; Jamehdor M; Ried T; Bartley J
    Am J Med Genet; 1998 Dec; 80(4):368-72. PubMed ID: 9856565
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterization of a neocentric supernumerary marker chromosome originating from the Xp distal region by FISH, CENP-C staining, and array CGH.
    Yu S; Barbouth D; Benke PJ; Warburton PE; Fan YS
    Cytogenet Genome Res; 2007; 116(1-2):141-5. PubMed ID: 17268194
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Forty-two supernumerary marker chromosomes (SMCs) in 43,273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies.
    Bartsch O; Loitzsch A; Kozlowski P; Mazauric ML; Hickmann G
    Eur J Hum Genet; 2005 Nov; 13(11):1192-204. PubMed ID: 16077735
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype.
    D'Amato Sizonenko L; Ng D; Oei P; Winship I
    Am J Med Genet; 2002 Jul; 111(1):19-26. PubMed ID: 12124728
    [TBL] [Abstract][Full Text] [Related]  

  • 13. FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22).
    Bartsch O; Rasi S; Hoffmann K; Blin N
    Eur J Hum Genet; 2005 May; 13(5):592-8. PubMed ID: 15756300
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Supernumerary marker chromosomes detected in 100,000 prenatal diagnoses: molecular cytogenetic studies and clinical significance.
    Huang B; Solomon S; Thangavelu M; Peters K; Bhatt S
    Prenat Diagn; 2006 Dec; 26(12):1142-50. PubMed ID: 17009345
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Trisomy 6q syndrome: a case with a << de novo >> 6q23 tandem duplication.
    Causio F; Fischetto R; Carnevale F; Pansini A; Rocchi M
    Genet Couns; 2001; 12(2):145-50. PubMed ID: 11491309
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
    Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
    Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterization of a supernumerary small marker X chromosome in two females with similar phenotypes.
    Tümer Z; Wolff D; Silahtaroglu AN; Orum A; Brøndum-Nielsen K
    Am J Med Genet; 1998 Feb; 76(1):45-50. PubMed ID: 9508064
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.
    Mark HF; Wyandt H; Huang XL; Milunsky JM
    Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pallister-Killian syndrome: tetrasomy of 12pter-->12p11.22 in a boy with an analphoid, inverted duplicated marker chromosome.
    Huang XL; Isabel de Michelena M; Leon E; Maher TA; McClure R; Milunsky A
    Clin Genet; 2007 Nov; 72(5):434-40. PubMed ID: 17894838
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two new cases of the Christchurch (Ch1) chromosome 21: evidence for clinical consequences of de novo deletion 21P-.
    Vorsanova SG; Yurov YB; Brusquant D; Carles E; Roizes G
    Tsitol Genet; 2002; 36(1):46-9. PubMed ID: 12012596
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.