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 *

136 related articles for article (PubMed ID: 4061490)

  • 1. NOR activity and centromere suppression related in a de novo fusion tdic(9;13)(p22;p13) chromosome in a child with del(9p) syndrome.
    Daniel A; Ekblom L; Phillips S; FitzGerald JM; Opitz JM
    Am J Med Genet; 1985 Nov; 22(3):577-84. PubMed ID: 4061490
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A tdic(5;15)(p31;p11) chromosome showing variation for constriction in the centromeric regions in a patient with the cri du chat syndrome.
    Dewald GW; Boros SJ; Conroy MM; Dahl RJ; Spurbeck JL; Vitek HA
    Cytogenet Cell Genet; 1979; 24(1):15-26. PubMed ID: 456039
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
    Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mental retardation, malformation syndrome andpartial 7p monosomy [45, XX, tdic (7;15) (p21;p11)].
    Nakagome Y; Teramura F; Katoaka K; Hosono F
    Clin Genet; 1976 Jun; 9(6):621-4. PubMed ID: 1277574
    [TBL] [Abstract][Full Text] [Related]  

  • 5. De novo del(7)(pter----p21.2::p15.2----qter) and craniosynostosis. Implications for critical segment assignment in the 7p2 monosomy syndrome.
    García-Esquivel L; García-Cruz D; Rivera H; Plascencia ML; Cantú JM
    Ann Genet; 1986; 29(1):36-8. PubMed ID: 3487273
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dicentric chromosome 13 and centromere inactivation.
    Schwartz S; Palmer CG; Weaver DD; Priest J
    Hum Genet; 1983; 63(4):332-7. PubMed ID: 6862437
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dissociation of tdic chromosomes: about a t(15;18)(p11;p11) leading to 18p monosomy.
    Garcia-Esquivel L; Rivera H; Sanchez-Corona J; Ramirez ML; Jimenez M; Cantú JM
    Ann Genet; 1987; 30(2):94-7. PubMed ID: 3499849
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Asymmetrical, reciprocal translocation (45,XX,tdic(9;17) (p21;p12).
    Waldenmaier C; Shibata K; Hirsch W
    J Ment Defic Res; 1975; 19(3-4):259-66. PubMed ID: 1214293
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation.
    Serra A; Bova R; Bellanova G; Chindemi A; Zappata S; Brahe C
    Am J Med Genet; 1997 Aug; 71(2):139-43. PubMed ID: 9217211
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Prenatal diagnosis of a de novo trisomy case 9q-47,XX,+9 del(q33----qter)].
    Cordier MP; Coicaud C; Thoulon JM; Robert JM; Germain D
    J Genet Hum; 1984 Dec; 32(5):351-61. PubMed ID: 6527131
    [TBL] [Abstract][Full Text] [Related]  

  • 11. New variant of chromosome 11.
    Aiello V; Ricci N; Palazzi P; D'Agostino G; Azzini G; Calzolari E
    Am J Med Genet; 1994 Apr; 50(3):294-5. PubMed ID: 8042675
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Direct duplication of 9p22-->p24 in a child with duplication 9p syndrome.
    Fujimoto A; Lin MS; Schwartz S
    Am J Med Genet; 1998 May; 77(4):268-71. PubMed ID: 9600733
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case with dicentric translocation between chromosome 9 and 18: confirmation by fluorescent in situ hybridization on metaphase spread.
    Isoyama K; Imai M; Ishikawa A; Fujita K; Suto Y; Shinohara T
    Acta Paediatr Jpn; 1995 Feb; 37(1):101-4. PubMed ID: 7754751
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
    Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
    [TBL] [Abstract][Full Text] [Related]  

  • 16. tdic(9;12): a nonrandom chromosome abnormality in childhood B-cell precursor acute lymphoblastic leukemia: a Pediatric Oncology Group Study.
    Carroll AJ; Raimondi SC; Williams DL; Behm FG; Borowitz M; Castleberry RP; Harris MB; Patterson RB; Pullen DJ; Crist WM
    Blood; 1987 Dec; 70(6):1962-5. PubMed ID: 3499945
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Karyotype, centric fusion polymorphism and chromosomal aberrations in captive-born mountain reedbuck (Redunca fulvorufula).
    Rubes J; Pagacova E; Kopecna O; Kubickova S; Cernohorska H; Vahala J; Di Berardino D
    Cytogenet Genome Res; 2007; 116(4):263-8. PubMed ID: 17431324
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A case of 9p- syndrome.
    Kuroki Y; Yokota S; Nakai H; Yamamoto Y; Matsui I
    Hum Genet; 1977 Aug; 38(1):107-11. PubMed ID: 903150
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Nucleolus organizer region--centromere translocation].
    de Blois MC; Rethoré MO; Lejeune J
    Ann Genet; 1989; 32(2):106-8. PubMed ID: 2757357
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Langer-Giedion syndrome with interstitial 8q-deletion.
    Zabel BU; Baumann WA
    Am J Med Genet; 1982 Mar; 11(3):353-8. PubMed ID: 7081298
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.