BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 17163527)

  • 1. A patient with duplication (7)(p22.1pter) characterized by array-CGH.
    Zahed L; Pramparo T; Farra C; Mikati M; Zuffardi O
    Am J Med Genet A; 2007 Jan; 143A(2):168-71. PubMed ID: 17163527
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A report of pure 7p duplication syndrome and review of the literature.
    Papadopoulou E; Sifakis S; Sarri C; Gyftodimou J; Liehr T; Mrasek K; Kalmanti M; Petersen MB
    Am J Med Genet A; 2006 Dec; 140(24):2802-6. PubMed ID: 17103460
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Xq chromosome duplication in males: clinical, cytogenetic and array CGH characterization of a new case and review.
    Cheng SF; Rauen KA; Pinkel D; Albertson DG; Cotter PD
    Am J Med Genet A; 2005 Jun; 135(3):308-13. PubMed ID: 15887264
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype.
    Sensi A; Prontera P; Buldrini B; Palma S; Aiello V; Gruppioni R; Calzolari E; Volinia S; Martini A
    Am J Med Genet A; 2008 Jan; 146A(1):110-5. PubMed ID: 18074369
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito and asymmetry.
    Schmidt H; Uhrig S; Lederer G; Murken J; Speicher MR; Schuffenhauer S
    J Med Genet; 2000 Oct; 37(10):804-7. PubMed ID: 11183189
    [No Abstract]   [Full Text] [Related]  

  • 6. Clinical and molecular characterization of chromosome 7p22.1 microduplication detected by array CGH.
    Chui JV; Weisfeld-Adams JD; Tepperberg J; Mehta L
    Am J Med Genet A; 2011 Oct; 155A(10):2508-11. PubMed ID: 21998864
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.
    Cai T; Yu P; Tagle DA; Xia J
    Am J Med Genet; 1999 Oct; 86(4):305-11. PubMed ID: 10494083
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pure direct duplication (12)(q24.1-->q24.2) in a child with Marcus Gunn phenomenon and multiple congenital anomalies.
    Doco-Fenzy M; Mauran P; Lebrun JM; Bock S; Bednarek N; Struski S; Albuisson J; Ardalan A; Collot N; Schneider A; Dastot-Le Moal F; Gaillard D; Goossens M
    Am J Med Genet A; 2006 Feb; 140(3):212-21. PubMed ID: 16411218
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Twins with mental retardation and an interstitial deletion 7q34q36.2 leading to the diagnosis of long QT syndrome.
    Bisgaard AM; Rackauskaite G; Thelle T; Kirchhoff M; Bryndorf T
    Am J Med Genet A; 2006 Mar; 140(6):644-8. PubMed ID: 16470702
    [No Abstract]   [Full Text] [Related]  

  • 11. Array comparative genomic hybridization analysis of a familial duplication of chromosome 13q: a recognizable syndrome.
    Mathijssen IB; Hoovers JM; Mul AN; Man HY; Ket JL; Hennekam RC
    Am J Med Genet A; 2005 Jul; 136(1):76-80. PubMed ID: 15889415
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A patient with duplication (7)(p15.3p22.3) and deletion (7)(p22.3pter) characterized by array-CGH.
    Geckinli BB; Aydin H; Karaman A
    Genet Couns; 2014; 25(4):405-12. PubMed ID: 25804019
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phenotype and micro-array characterization of duplication 11q22.1-q25 and review of the literature.
    Ben-Abdallah-Bouhjar I; Mougou-Zerelli S; Hannachi H; Ben-Khelifa H; Soyah N; Labalme A; Sanlaville D; Elghezal H; Saad A
    Gene; 2013 Apr; 519(1):135-41. PubMed ID: 23403231
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Duplication of distal 20q: clinical, cytogenetic and array CGH. Characterization of a new case.
    Iglesias A; Rauen KA; Albertson DG; Pinkel D; Cotter PD
    Clin Dysmorphol; 2006 Jan; 15(1):19-23. PubMed ID: 16317302
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Trisomy 20q caused by interstitial duplication 20q13.2: clinical report and literature review.
    Blanc P; Gouas L; Francannet C; Giollant M; Vago P; Goumy C
    Am J Med Genet A; 2008 May; 146A(10):1307-11. PubMed ID: 18384146
    [TBL] [Abstract][Full Text] [Related]  

  • 17. No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrome patients.
    Miyake N; Shimokawa O; Harada N; Sosonkina N; Okubo A; Kawara H; Okamoto N; Ohashi H; Kurosawa K; Naritomi K; Kaname T; Nagai T; Shotelersuk V; Hou JW; Fukushima Y; Kondoh T; Matsumoto T; Shinoki T; Kato M; Tonoki H; Nomura M; Yoshiura K; Kishino T; Ohta T; Niikawa N; Matsumoto N
    Am J Med Genet A; 2006 Feb; 140(3):291-3. PubMed ID: 16278908
    [No Abstract]   [Full Text] [Related]  

  • 18. Duplication of 7p: further delineation of the phenotype and restriction of the critical region to the distal part of the short arm.
    Reish O; Berry SA; Dewald G; King RA
    Am J Med Genet; 1996 Jan; 61(1):21-5. PubMed ID: 8741912
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotypic spectrum of interstitial 7p duplication in mosaic and non-mosaic forms.
    Cox H; Stewart H; Hall L; Donnai D
    Am J Med Genet; 2002 May; 109(4):306-10. PubMed ID: 11992485
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients.
    Martinet D; Filges I; Besuchet Schmutz N; Morris MA; Gaide AC; Dahoun S; Bottani A; Addor MC; Antonarakis SE; Beckmann JS; Béna F
    Am J Med Genet A; 2008 Aug; 146A(16):2094-102. PubMed ID: 18629875
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.