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 *

178 related articles for article (PubMed ID: 9272714)

  • 1. A patient with Edwards syndrome caused by a rare pseudodicentric chromosome 18 of paternal origin.
    Gravholt CH; Bugge M; Strømkjaer H; Caprani M; Henriques U; Petersen MB; Brandt CA
    Clin Genet; 1997 Jul; 52(1):56-60. PubMed ID: 9272714
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pseudodicentric chromosome 18 diagnosed by chromosome painting and primed in situ labelling (PRINS).
    Brandt CA; Djernes B; Strømkjaer H; Petersen MB; Pedersen S; Hindkjaer J; Brinch-Iversen J; Bruun-Petersen G
    J Med Genet; 1994 Feb; 31(2):99-102. PubMed ID: 8182728
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Partial trisomy of the short arm of chromosome 18 due to inversion duplication and direct duplication.
    Moog U; Engelen JJ; de Die-Smulders CE; Albrechts JC; Loneus WH; Haagen AA; Raven EJ; Hamers AJ
    Clin Genet; 1994 Dec; 46(6):423-9. PubMed ID: 7889659
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Partial trisomy 13q22-->qter and monosomy 18q21-->qter as a result of familial translocation.
    Cekada S; Kilvain S; Brajenović-Milić B; Brecević L; Kirincić-Paucić E; Franulović J
    Acta Paediatr; 1999 Jun; 88(6):675-8. PubMed ID: 10419257
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Isodicentric chromosome 18 in an abnormal infant using chromosome specific DNA probe.
    Meguid NA; Habibian R
    Clin Genet; 1992 May; 41(5):225-8. PubMed ID: 1606710
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
    Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
    Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter-->22q12.1: clinical, cytogenetic and molecular observations.
    Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Maher TA; Quadrelli R
    Eur J Med Genet; 2008; 51(4):332-42. PubMed ID: 18316257
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
    Oner G; Jauch A; Eggermann T; Hardwick R; Kirsch S; Schiebel K; Rappold G; Robson L; Smith A
    Am J Med Genet; 2000 May; 92(2):101-6. PubMed ID: 10797432
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A case of duplication of 13q32-->qter and deletion of 18p11.32-->pter with mild phenotype: Patau syndrome and duplications of 13q revisited.
    Helali N; Iafolla AK; Kahler SG; Qumsiyeh MB
    J Med Genet; 1996 Jul; 33(7):600-2. PubMed ID: 8818949
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The origin of cytologically unidentifiable chromosome abnormalities: six cases ascertained by targeted chromosome-band painting.
    Ohta T; Tohma T; Soejima H; Fukushima Y; Nagai T; Yoshiura K; Jinno Y; Niikawa N
    Hum Genet; 1993 Aug; 92(1):1-5. PubMed ID: 8365720
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18.
    Boghosian-Sell L; Mewar R; Harrison W; Shapiro RM; Zackai EH; Carey J; Davis-Keppen L; Hudgins L; Overhauser J
    Am J Hum Genet; 1994 Sep; 55(3):476-83. PubMed ID: 8079991
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Molecular cytogenetic determination of a deletion/duplication of 1q that results in a trisomy 18 syndrome-like phenotype.
    Mewar R; Harrison W; Weaver DD; Palmer C; Davee MA; Overhauser J
    Am J Med Genet; 1994 Aug; 52(2):178-83. PubMed ID: 7802005
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome).
    Nöthen MM; Eggermann T; Erdmann J; Eiben B; Hofmann D; Propping P; Schwanitz G
    Hum Genet; 1993 Oct; 92(4):347-9. PubMed ID: 8225314
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Partial trisomy 13 in an infant with a mild phenotype: application of fluorescence in situ hybridization in cytogenetic syndromes.
    Begovic D; Hitrec V; Lasan R; Letica L; Baric I; Sarnavka V; Galic S
    Croat Med J; 1998 Jun; 39(2):212-5. PubMed ID: 9575279
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterization of a derivative chromosome 17 by fish-technique.
    Ramesh KH; Shah HO; Sherman J; Lin JH; Verma RS
    Ann Genet; 1996; 39(3):177-80. PubMed ID: 8839891
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18.
    Quadrelli R; Quadrelli A; Milunsky A; Zou YS; Huang XL; Viera E; Mechoso B; Bellini S; Costabel M; Vaglio A
    Genet Test Mol Biomarkers; 2009 Jun; 13(3):387-93. PubMed ID: 19473082
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting.
    Coêlho KE; Egashira M; Kato R; Fujimoto M; Matsumoto N; Rerkamnuaychoke B; Abe K; Harada N; Ohashi H; Fukushima Y; Niikawa N
    Am J Med Genet; 1996 Jun; 63(3):468-71. PubMed ID: 8737654
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.