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 *

216 related articles for article (PubMed ID: 8287190)

  • 1. Partial 6q monosomy/partial 12q trisomy in a child with features of Kabuki make-up syndrome.
    Jardine PE; Burvill-Holmes LC; Schutt WH; Lunt PW
    Clin Dysmorphol; 1993 Jul; 2(3):269-73. PubMed ID: 8287190
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
    Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
    Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.
    Ausems MG; Van Spijker HG; Dijkhuis HJ; Swanenburg De Veye HF; Bijlsma JB
    Genet Couns; 1996; 7(1):61-5. PubMed ID: 8652090
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A fourteen years follow-up of a case of partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of chromosome 12: clinical, cytogenetic and molecular observations.
    Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Quadrelli R
    Eur J Med Genet; 2007; 50(3):224-32. PubMed ID: 17329177
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Kabuki syndrome and trisomy 10p.
    Utine GE; Alanay Y; Atkaş D; Boduroğlu K; Alikaşifoğlu M; Tunçbilek E
    Genet Couns; 2008; 19(3):291-300. PubMed ID: 18990985
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
    Lukusa T; van den Berghe L; Smeets E; Fryns JP
    Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial 4q duplication due to inherited der(20), t(4;20)(q25;q13)mat.
    Sparkes RS; Francke U; Muller H; Toomey K
    Ann Genet; 1977 Mar; 20(1):31-5. PubMed ID: 302670
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Two patients with chromosome 6q terminal deletions with breakpoints at q24.3 and q25.3.
    Meng J; Fujita H; Nagahara N; Kashiwai A; Yoshioka Y; Funato M
    Am J Med Genet; 1992 Jul; 43(4):747-50. PubMed ID: 1621768
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pure trisomy 2p syndrome in two siblings with an unbalanced translocation and minimal terminal 12q monosomy characterized by high-density microarray.
    Martínez-Juárez A; Uribe-Figueroa L; Quintana-Palma M; Razo-Aguilera G; Sevilla-Montoya R
    Cytogenet Genome Res; 2014; 142(4):249-54. PubMed ID: 24751616
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Rethoré syndrome (9p trisomy) with unusual karyotype: 46,XX,-9, + der 9p, t(9;9)mat].
    Di Cesare D; Paludetto R; Casullo C; Pagano L; Stabile M; Sicolo A; Ventruto V
    Minerva Pediatr; 1980 Dec; 32(23):1349-52. PubMed ID: 7219376
    [No Abstract]   [Full Text] [Related]  

  • 11. Malformation syndrome of duplication 12q24.1 leads to qter.
    Melnyk AR; Weiss L; Van Dyke DL; Jarvi P
    Am J Med Genet; 1981; 10(4):357-65. PubMed ID: 7332029
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two cases with partial trisomy 9: cytogenetic and clinical findings.
    Ozer O; Derbent M; Sahin FI; Yilmaz Z
    Genet Couns; 2010; 21(2):205-13. PubMed ID: 20681221
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literature.
    Wang CB; Lin SP; Chen CP; Chen YJ; Lee CC
    Genet Couns; 2006; 17(4):435-40. PubMed ID: 17375530
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
    Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
    Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Trisomy 20q caused by der(4) t(4;20) (q35;q13.1): report of a new patient and review of the literature.
    Plotner PL; Smith JL; Northrup H
    Am J Med Genet; 2002 Jul; 111(1):71-5. PubMed ID: 12124739
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ring chromosome 22 resulting in partial monosomy in a mentally retarded boy.
    Gibbons B; Tan SY; Tam PY
    Singapore Med J; 1999 Apr; 40(4):273-5. PubMed ID: 10487083
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
    Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W
    Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Precocious puberty associated with partial trisomy 18q and monosomy 11q.
    Mutesa L; Hellin AC; Jamar M; Pierquin G; Bours V; Verloes A
    Genet Couns; 2007; 18(2):201-7. PubMed ID: 17710872
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Partial trisomy 1q and monosomy 18q due to a de novo t(1;18)(q25;q23).
    Solé MT; Rivera H; Sánchez-Corona J; Plascencia L; Cantú JM
    Ann Genet; 1983; 26(2):120-2. PubMed ID: 6604487
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.