These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

274 related articles for article (PubMed ID: 9856565)

  • 1. 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]  

  • 2. Tetrasomy 15q25-->qter: cytogenetic and molecular characterization of an analphoid supernumerary marker chromosome.
    Rowe AG; Abrams L; Qu Y; Chen E; Cotter PD
    Am J Med Genet; 2000 Aug; 93(5):393-8. PubMed ID: 10951463
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker.
    Dufke A; Walczak C; Liehr T; Starke H; Trifonov V; Rubtsov N; Schöning M; Enders H; Eggermann T
    Eur J Hum Genet; 2001 Aug; 9(8):572-6. PubMed ID: 11528501
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13.
    Tonnies H; Gerlach A; Heineking B; Starke H; Neitzel H; Neumann LM
    Cytogenet Genome Res; 2006; 114(3-4):325-9. PubMed ID: 16954674
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mosaic tetrasomy 8q: inverted duplication of 8q23.3qter in an analphoid marker.
    Reddy KS; Sulcova V; Schwartz S; Noble JE; Phillips J; Brasel JA; Huff K; Lin HJ
    Am J Med Genet; 2000 May; 92(1):69-76. PubMed ID: 10797426
    [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. Application of fluorescence in situ hybridization to the identification of different marker chromosomes.
    Verschraegen-Spae MR; Quack B; Rousseaux S; Pison H; Messiaen L; De Paepe A; Lespinasse J
    Ann Genet; 1998; 41(1):5-10. PubMed ID: 9599644
    [TBL] [Abstract][Full Text] [Related]  

  • 9. First prenatally detected small supernumerary neocentromeric derivative chromosome 13 resulting in a non-mosaic partial tetrasomy 13q.
    Mascarenhas A; Matoso E; Saraiva J; Tönnies H; Gerlach A; Julião MJ; Melo JB; Carreira IM
    Cytogenet Genome Res; 2008; 121(3-4):293-7. PubMed ID: 18758175
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors.
    Hu J; McPherson E; Surti U; Hasegawa SL; Gunawardena S; Gollin SM
    Am J Med Genet; 2002 Nov; 113(1):82-8. PubMed ID: 12400070
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
    Spikes AS; Hegmann K; Smith JL; Shaffer LG
    Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Fluorescence in situ hybridization (FISH) of a whole-arm translocation involving chromosomes 18 and 20 with alpha-satellite DNA probes: detection of a centromeric DNA break?
    Cantú ES; Khan TA; Pai GS
    Am J Med Genet; 1992 Oct; 44(3):340-4. PubMed ID: 1488982
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
    Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Marker chromosome 21 identified by microdissection and FISH.
    Sun Y; Rubinstein J; Soukup S; Palmer CG
    Am J Med Genet; 1995 Mar; 56(2):151-4. PubMed ID: 7542834
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mosaic tetrasomy 15q25-->qter in a newborn infant with multiple anomalies.
    Van den Enden A; Verschraegen-Spae MR; Van Roy N; Decaluwe W; De Praeter C; Speleman F
    Am J Med Genet; 1996 Jun; 63(3):482-5. PubMed ID: 8737657
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 10p duplication characterized by fluorescence in situ hybridization.
    Wiktor A; Feldman GL; Kratkoczki P; Ditmars DM; Van Dyke DL
    Am J Med Genet; 1994 Sep; 52(3):315-8. PubMed ID: 7528972
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequence.
    Assumpção JG; Berkofsky-Fessler W; Viguetti Campos N; Trevas Maciel-Guerra A; Li S; Melaragno MI; Palandi de Mello M; Warburton PE
    Am J Med Genet; 2002 Dec; 113(3):263-7. PubMed ID: 12439894
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.