BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

612 related articles for article (PubMed ID: 7645598)

  • 1. Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two cases.
    Schimmenti LA; Higgins RR; Mendelsohn NJ; Casey TM; Steinberger J; Mammel MC; Wiesner GL
    Am J Med Genet; 1995 May; 57(1):52-6. PubMed ID: 7645598
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Partial trisomy 8p (8p11.2-->pTER) and deletion of 13q (13q32-->qTER): case report.
    Yeşilyurt A; Dilli D; Oguz S; Dilmen U; Altug N; Candemir Z
    Genet Couns; 2011; 22(1):35-40. PubMed ID: 21614986
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Partial trisomy and partial monosomy of the distal long arm of chromosome 4: patient report and literature review.
    Frints SG; Schrander-Stumpel CT; Engelen JJ; Da Costa AJ; Fryns JP
    Genet Couns; 1996; 7(2):135-42. PubMed ID: 8831133
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p.
    Okten G; Sezer O; Günes S; Küçüködük S; Oğur G
    Genet Couns; 2009; 20(4):341-7. PubMed ID: 20162869
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20.
    Okada M; Usami A; Okajima K; Yamada M; Yamaguchi Y; Umezaki I; Matsuda Y; Ohta H
    Congenit Anom (Kyoto); 2005 Dec; 45(4):161-4. PubMed ID: 16359498
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter.
    Cohn AC; Kearns LS; Savarirayan R; Ryan J; Craig JE; Mackey DA
    Ophthalmic Genet; 2005 Mar; 26(1):45-53. PubMed ID: 15823925
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.
    Brisset S; Joly G; Ozilou C; Lapierre JM; Gosset P; LeLorc'h M; Raoul O; Turleau C; Vekemans M; Romana SP
    Am J Med Genet; 2002 Dec; 113(4):339-45. PubMed ID: 12457405
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. DiGeorge syndrome and partial monosomy 10p: case report and review.
    Schuffenhauer S; Seidel H; Oechsler H; Belohradsky B; Bernsau U; Murken J; Meitinger T
    Ann Genet; 1995; 38(3):162-7. PubMed ID: 8540688
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Partial monosomy 3p (3p26.2 --> pter) and partial trisomy 5q (5q34 --> qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay.
    Chen CP; Lin SP; Chen MR; Su YN; Chern SR; Liu YP; Su JW; Lee MS; Wang W
    Genet Couns; 2012; 23(3):405-13. PubMed ID: 23072190
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation.
    Serra A; Bova R; Bellanova G; Chindemi A; Zappata S; Brahe C
    Am J Med Genet; 1997 Aug; 71(2):139-43. PubMed ID: 9217211
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
    Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Trisomy 22: no longer an enigma.
    Kukolich MK; Kulharya A; Jalal SM; Drummond-Borg M
    Am J Med Genet; 1989 Dec; 34(4):541-4. PubMed ID: 2624265
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Duplication of part of chromosome 1q: clinical report and review of literature.
    Michels VV; Berseth CL; O'Brien JF; Dewald G
    Am J Med Genet; 1984 May; 18(1):125-34. PubMed ID: 6430083
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
    Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Interstitial deletion of 8q21-->22 associated with minor anomalies, congenital heart defect, and Dandy-Walker variant.
    Donahue ML; Ryan RM
    Am J Med Genet; 1995 Mar; 56(1):97-100. PubMed ID: 7747796
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of a derivative chromosome 17 by fish-technique.
    Ramesh KH; Shah HO; Sherman J; Lin JH; Verma RS
    Ann Genet; 1996; 39(3):177-80. PubMed ID: 8839891
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Infant with del(3) (p25-pter): karyotype-phenotype correlation and review of previously reported cases.
    Nienhaus H; Mau U; Zang KD
    Am J Med Genet; 1992 Nov; 44(5):573-5. PubMed ID: 1481811
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 31.