BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

52 related articles for article (PubMed ID: 9286456)

  • 1. Cytogenetic and molecular analyses of de novo translocation dic(9;13)(p11.2;p12) in an infertile male.
    Wiland E; Olszewska M; Georgiadis A; Huleyuk N; Panasiuk B; Zastavna D; Yatsenko SA; Jedrzejczak P; Midro AT; Yatsenko AN; Kurpisz M
    Mol Cytogenet; 2014 Feb; 7(1):14. PubMed ID: 24559467
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case.
    Wafa A; Jarjour RA; Aljapawe A; ALmedania S; Liehr T; Melo JB; Carreira IM; Othman MAK; Al-Achkar W
    Mol Cytogenet; 2020; 13():29. PubMed ID: 32670411
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 18p Deletion Syndrome With a 45, XY, t (14;18) (p11.1; p11.1), Karyotype.
    Ashgan B; Al-Agha A; Alhamdani Y; Shazly MA
    Cureus; 2024 Mar; 16(3):e55539. PubMed ID: 38576635
    [TBL] [Abstract][Full Text] [Related]  

  • 4. dic(7;9)(p11-13;p11).
    Underdown MJ; Russell TB; Pettenati MJ; Kram DE
    Atlas Genet Cytogenet Oncol Haematol; 2006; 10(2):110-111. PubMed ID: 34531928
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 18p Deletion Syndrome Originating from Rare Unbalanced Whole-Arm Translocation between Chromosomes 13 and 18: A Case Report and Literature Review.
    Choi JY; Moon JU; Yoon DH; Yim J; Kim M; Jung MH
    Children (Basel); 2022 Jul; 9(7):. PubMed ID: 35883971
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Human Chromosome 18 and Acrocentrics: A Dangerous Liaison.
    Villa N; Redaelli S; Sala E; Conconi D; Romitti L; Manfredini E; Crosti F; Roversi G; Lavitrano M; Rodeschini O; Recalcati MP; Piazza R; Dalprà L; Riva P; Bentivegna A
    Int J Mol Sci; 2021 May; 22(11):. PubMed ID: 34073228
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Anterior Pituitary Aplasia in an Infant with Ring Chromosome 18p Deletion.
    Bellfield EJ; Chan J; Durrin S; Lindgren V; Shad Z; Boucher-Berry C
    Case Rep Endocrinol; 2016; 2016():2853178. PubMed ID: 27843654
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Monosomy 18p.
    Turleau C
    Orphanet J Rare Dis; 2008 Feb; 3():4. PubMed ID: 18284672
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial whole-arm translocations (1;19), (9;13), and (12;21): a review of 101 constitutional exchanges.
    Vázquez-Cárdenas A; Vásquez-Velásquez AI; Barros-Núñez P; Mantilla-Capacho J; Rocchi M; Rivera H
    J Appl Genet; 2007; 48(3):261-8. PubMed ID: 17666779
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion.
    Prontera P; Aiello V; Toschi M; Turci A; Gruppioni R; Buldrini B; Zago S; Bonfatti A; Donti E; Calzolari E; Sensi A
    Genet Couns; 2007; 18(3):309-15. PubMed ID: 18019372
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Reciprocal translocation t(1;15)(p36.2;p11.2): confirmation of a suggestive cytogenetic diagnosis by in situ hybridization and clinical case report on resulting monosomy (1p).
    Barbi G; Kennerknecht I; Klett C
    Am J Med Genet; 1992 Jul; 43(4):722-5. PubMed ID: 1621764
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p.
    Wang JC; Nemana L; Kou SY; Habibian R; Hajianpour MJ
    Am J Med Genet; 1997 Sep; 71(4):463-6. PubMed ID: 9286456
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p.
    McGhee EM; Qu Y; Wohlferd MM; Goldberg JD; Norton ME; Cotter PD
    Clin Genet; 2001 Apr; 59(4):274-8. PubMed ID: 11298684
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.
    Tharapel AT; Qumsiyeh MB; Martens PR; Tharapel SA; Dalton JD; Ward JC; Wilroy RS
    Am J Med Genet; 1991 Jul; 40(1):117-20. PubMed ID: 1887840
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
    Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
    [TBL] [Abstract][Full Text] [Related]  

  • 16.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 17.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 18.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.