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 *

122 related articles for article (PubMed ID: 21271652)

  • 1. Pure and complete 12p trisomy due to a maternal centric fission of chromosome 12.
    Cetin Z; Mihci E; Yakut S; Keser I; Karauzum SB; Luleci G
    Am J Med Genet A; 2011 Feb; 155A(2):349-52. PubMed ID: 21271652
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Centric fission, centromere-telomere fusion and isochromosome formation: a possible origin of a de novo 12p trisomy.
    Rivera H; García-Esquivel L; Jiménez-Sáinz M; Vaca G; Ibarra B; Cantú JM
    Clin Genet; 1987 Jun; 31(6):393-8. PubMed ID: 3621643
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genotype/phenotype analysis in a patient with pure and complete trisomy 12p.
    Zumkeller W; Volleth M; Muschke P; Tönnies H; Heller A; Liehr T; Wieacker P; Stumm M
    Am J Med Genet A; 2004 Sep; 129A(3):261-4. PubMed ID: 15326625
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cytogenetic and molecular analysis in trisomy 12p.
    Allen TL; Brothman AR; Carey JC; Chance PF
    Am J Med Genet; 1996 May; 63(1):250-6. PubMed ID: 8723118
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical, cytogenetic, and molecular observations in a patient with Pallister-Killian-syndrome with an unusual karyotype.
    Leube B; Majewski F; Gebauer J; Royer-Pokora B
    Am J Med Genet A; 2003 Dec; 123A(3):296-300. PubMed ID: 14608653
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes.
    Pauli S; Schmidt T; Funke R; Zoll B; Burfeind P; Dybowski U; Shoukier M; Bartels I
    Eur J Med Genet; 2012; 55(8-9):480-4. PubMed ID: 22677035
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical and molecular cytogenetic observations in three cases of "trisomy 12p syndrome".
    Rauch A; Trautmann U; Pfeiffer RA
    Am J Med Genet; 1996 May; 63(1):243-9. PubMed ID: 8723117
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular Delineation of Partial Trisomy 14q and Partial Trisomy 12p in a Patient with Dysmorphic Features, Heart Defect and Developmental Delay.
    Bose D; Krishnamurthy V; Venkatesh KS; Aiyaz M; Shetty M; Rao SN; Kutty AV
    Cytogenet Genome Res; 2015; 145(1):14-8. PubMed ID: 25896599
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
    Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
    Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Report on 3 patients with 12p duplication including GRIN2B.
    Poirsier C; Landais E; Bednarek N; Nobecourt JM; Khoury M; Schmidt P; Morville P; Gruson N; Clomes S; Michel N; Riot A; Manjeongean C; Gaillard D; Doco-Fenzy M
    Eur J Med Genet; 2014 Apr; 57(5):185-94. PubMed ID: 24503147
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 12P trisomy: a syndrome?
    Hoo JJ
    Ann Genet; 1976 Dec; 19(4):261-3. PubMed ID: 1087857
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case.
    Tuğ E; Yirmibeş Karaoğuz M; Kayhan G; Ergün MA; Perçin FE
    Am J Med Genet A; 2014 Jul; 164A(7):1770-6. PubMed ID: 24677787
    [TBL] [Abstract][Full Text] [Related]  

  • 13. SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangement.
    Magri C; Marchina E; Bertini V; Traversa M; Savio G; Pilotta A; Piovani G
    BMC Med Genet; 2015 Jul; 16():47. PubMed ID: 26149167
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Centromere-telomere (12;8p) fusion, telomeric 12q translocation, and i(12p) trisomy.
    Rivera H; Vásquez AI; Perea FJ
    Clin Genet; 1999 Feb; 55(2):122-6. PubMed ID: 10189090
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial trisomy for 5q and monosomy for 12p in a liveborn child as a result of a complex five breakpoint chromosome rearrangement in a parent.
    Van Der Burgt CJ; Merkx GF; Janssen AH; Mulder JC; Suijkerbuijk RF; Smeets DF
    J Med Genet; 1992 Oct; 29(10):739-41. PubMed ID: 1433237
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pure partial trisomy 4q syndrome in a child with der(9)ins(9;4)(q34.3;q26q35.2)mat.
    Topcu V; Ilgin-Ruhi H; Yurur-Kutlay N; Ekici C; Vicdan A; Tukun FA
    Genet Couns; 2014; 25(1):1-6. PubMed ID: 24783648
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A father and son with mental retardation, a characteristic face, inv(12), and insertion trisomy 12p12.3-p11.2.
    Liang D; Wu L; Pan Q; Harada N; Long Z; Xia K; Yoshiura K; Dai H; Niikawa N; Cai F; Xia J
    Am J Med Genet A; 2006 Feb; 140(3):238-44. PubMed ID: 16411213
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Trisomy 12p and monosomy 4p: phenotype-genotype correlation.
    Benussi DG; Costa P; Zollino M; Murdolo M; Petix V; Carrozzi M; Pecile V
    Genet Test Mol Biomarkers; 2009 Apr; 13(2):199-204. PubMed ID: 19378504
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.