BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 16103663)

  • 1. Pure trisomy 19p syndrome in an infant with an extra ring chromosome.
    Novelli A; Ceccarini C; Bernardini L; Zuccarello D; Digilio MC; Mingarelli R; Dallapiccola B
    Cytogenet Genome Res; 2005; 111(2):182-5. PubMed ID: 16103663
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
    Chantot-Bastaraud S; Muti C; Pipiras E; Routon MC; Roubergue A; Burglen L; Siffroi JP; Simon-Bouy B
    Ann Genet; 2004; 47(3):241-9. PubMed ID: 15337469
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Trisomy 12p syndrome: de novo occurrence of mosaic trisomy 12p in a mentally retarded boy.
    Kondo I; Hamaguchi H; Haneda T
    Hum Genet; 1979 Jan; 46(2):135-40. PubMed ID: 422196
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
    Chen H; Tuck-Muller CM; Batista DA; Wertelecki W
    Am J Med Genet; 1995 Mar; 56(2):219-33. PubMed ID: 7625449
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies: molecular mapping of a new syndrome by fluorescent in situ hybridization and microsatellites to 16q13 (D16S419-D16S503).
    Stratakis CA; Lafferty A; Taymans SE; Gafni RI; Meck JM; Blancato J
    J Clin Endocrinol Metab; 2000 Sep; 85(9):3396-401. PubMed ID: 10999840
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Distal 14q trisomy].
    Turleau C; de Grouchy J; Chavin-Colin F; Denavit MF; Le Touzé P
    Ann Genet; 1983; 26(3):165-70. PubMed ID: 6606379
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype.
    Tan-Sindhunata G; Castedo S; Leegte B; Mulder I; vd Veen AY; vd Hout AH; Wiersma TJ; van Essen AJ
    Am J Med Genet; 2000 May; 92(2):147-52. PubMed ID: 10797441
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Proximal trisomy 19q. Interstitial deletion and ring chromosome derived from 19q].
    Klein F; Schuck D; Noël B; Stoessel J; Vibert M
    Pediatrie; 1989; 44(9):717-20. PubMed ID: 2622712
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Interstitial deletion and ring chromosome derived from 19q. Proximal 19q trisomy phenotype.
    Quack B; Van Roy N; Verschraegen-Spae MR; Klein F
    Ann Genet; 1992; 35(4):241-4. PubMed ID: 1296524
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
    Akbas E; Polat S; Karakas-Celik S; Altintas ZM; Yildirim M; Yilgor E
    Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CGH and direct diagnosis of mosaic structural chromosomal abnormalities: description of a mosaic ring chromosome 17 and review of the literature.
    Dupont C; Pipiras E; Chantot-Bastaraud S; Verloes A; Baumann C; Wolf JP; Benzacken B
    Eur J Hum Genet; 2003 Jun; 11(6):452-6. PubMed ID: 12774038
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features.
    Mégarbané A; Souraty N; Theophile D; Vekemans M; Samaras L; Ghorayeb Z
    Ann Genet; 1997; 40(1):55-9. PubMed ID: 9150851
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome.
    Nadal M; Milà M; Pritchard M; Mur A; Pujals J; Blouin JL; Antonarakis SE; Ballesta F; Estivill X
    Hum Genet; 1996 Oct; 98(4):460-6. PubMed ID: 8792823
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
    de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
    Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Segregation of a t(1;3) translocation in multiple affected family members with both types of adjacent-1 segregants.
    Kozma C; Slavotinek AM; Meck JM
    Am J Med Genet A; 2004 Jan; 124A(2):118-28. PubMed ID: 14699608
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
    Mach M; Windpassinger C; Wagner K; Kroisel PM; Petek E
    Genet Couns; 2007; 18(1):9-16. PubMed ID: 17515297
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype.
    D'Amato Sizonenko L; Ng D; Oei P; Winship I
    Am J Med Genet; 2002 Jul; 111(1):19-26. PubMed ID: 12124728
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.