BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 15666303)

  • 21. Trisomy of 8q22.3 approximately q23-qter following an unbalanced 1;8 translocation in a boy with multiple anomalies.
    Ergun MA; Balci S; Konaç E; Kan D; Menevşe S; Bartsch O
    Turk J Pediatr; 2004; 46(4):384-7. PubMed ID: 15641279
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Phenotypic features of a boy with trisomy of 16q22-->qter due to paternal Y; 16 translocation.
    Tsien F; Morava E; Talarski A; Marble M
    Clin Dysmorphol; 2005 Oct; 14(4):177-181. PubMed ID: 16155418
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Detection of an unexpected subtelomeric 15q26.2 --> qter deletion in a little girl: clinical and cytogenetic studies.
    Pinson L; Perrin A; Plouzennec C; Parent P; Metz C; Collet M; Le Bris MJ; Douet-Guilbert N; Morel F; De Braekeleer M
    Am J Med Genet A; 2005 Oct; 138A(2):160-5. PubMed ID: 16114049
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Duplication of medial 15q confirmed by FISH.
    Browne CE; Hatchwell E; Protopapas A; Ramos J
    J Med Genet; 2000 Aug; 37(8):E10. PubMed ID: 10922390
    [No Abstract]   [Full Text] [Related]  

  • 25. Distal 5q trisomy resulting from an X;5 translocation detected by chromosome painting.
    Abuelo DN; Ahsanuddin AN; Mark HF
    Am J Med Genet; 2000 Oct; 94(5):392-9. PubMed ID: 11050625
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation.
    Stankiewicz P; Kuechler A; Eller CD; Sahoo T; Baldermann C; Lieser U; Hesse M; Gläser C; Hagemann M; Yatsenko SA; Liehr T; Horsthemke B; Claussen U; Marahrens Y; Lupski JR; Hansmann I
    Am J Med Genet A; 2006 Mar; 140(5):442-52. PubMed ID: 16470732
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Tetrasomy 15q25.2→qter identified with SNP microarray in a patient with multiple anomalies including complex cardiovascular malformation.
    George-Abraham JK; Zimmerman SL; Hinton RB; Marino BS; Witte DP; Hopkin RJ
    Am J Med Genet A; 2012 Aug; 158A(8):1971-6. PubMed ID: 22711292
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mosaic tetrasomy 15q25-->qter in a newborn infant with multiple anomalies.
    Van den Enden A; Verschraegen-Spae MR; Van Roy N; Decaluwe W; De Praeter C; Speleman F
    Am J Med Genet; 1996 Jun; 63(3):482-5. PubMed ID: 8737657
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Maternal origin of extra marker chromosome 1Q31.1-qter and 13pter-q12.12 in a child with dysmorhic features.
    Rao VB; Kerketta L; Korgaonkar S; Ghosh K; Mohanty D
    Genet Couns; 2005; 16(2):139-43. PubMed ID: 16082769
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Overgrowth and trisomy 15q26.1-qter including the IGF1 receptor gene: report of two families and review of the literature.
    Faivre L; Gosset P; Cormier-Daire V; Odent S; Amiel J; Giurgea I; Nassogne MC; Pasquier L; Munnich A; Romana S; Prieur M; Vekemans M; De Blois MC; Turleau C
    Eur J Hum Genet; 2002 Nov; 10(11):699-706. PubMed ID: 12404101
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISH.
    Petek E; Köstl G; Mutz I; Wagner K; Kroisel PM
    Clin Dysmorphol; 2000 Jan; 9(1):55-7. PubMed ID: 10649799
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Tandem translocation of chromosomes 22 and 15 with two preserved satellite stalk regions and deletion 22q13.3-qter.
    Lee KA; Kim SH; Lee MH; Law ME; Jalal SM
    Am J Med Genet; 2001 Dec; 104(4):291-4. PubMed ID: 11754062
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of an unusual marker chromosome by spectral karyotyping.
    Huang B; Ning Y; Lamb AN; Sandlin CJ; Jamehdor M; Ried T; Bartley J
    Am J Med Genet; 1998 Dec; 80(4):368-72. PubMed ID: 9856565
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation.
    de Carvalho AF; da Silva Bellucco FT; Kulikowski LD; Toralles MB; Melaragno MI
    Hum Genet; 2008 Nov; 124(4):387-92. PubMed ID: 18777129
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Phenotype-genotype correlation of a patient with a "balanced" translocation 9;15 and cryptic 9q34 duplication and 15q21q25 deletion.
    Papadopoulou E; Sismani C; Christodoulou C; Ioannides M; Kalmanti M; Patsalis P
    Am J Med Genet A; 2010 Jun; 152A(6):1515-22. PubMed ID: 20503328
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Karyotype/phenotype correlation in partial trisomies of the long arm of chromosome 16: case report and review of literature.
    Laus AC; Baratela WA; Laureano LA; Santos SA; Huber J; Ramos ES; Rebelo CC; Squire JA; Martelli L
    Am J Med Genet A; 2012 Apr; 158A(4):821-7. PubMed ID: 22354628
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Proximal and distal 15q25.2 microdeletions-genotype-phenotype delineation of two neurodevelopmental susceptibility loci.
    Doelken SC; Seeger K; Hundsdoerfer P; Weber-Ferro W; Klopocki E; Graul-Neumann L
    Am J Med Genet A; 2013 Jan; 161A(1):218-24. PubMed ID: 23239641
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The phenotype of partial dup(7q) reconsidered: a report of five new cases.
    Forabosco A; Baroncini A; Dalpra L; Chessa L; Giannotti A; Maccagnani F; Dallapiccola B
    Clin Genet; 1988 Jul; 34(1):48-59. PubMed ID: 3409538
    [TBL] [Abstract][Full Text] [Related]  

  • 40. De novo mosaic add(3) characterized to be trisomy 14q31-qter using spectral karyotyping and subtelomeric probes.
    Reddy KS; Sulcova V; Young H; Blancato JK; Haddad BR
    Am J Med Genet; 1999 Feb; 82(4):318-21. PubMed ID: 10051165
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.