BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

167 related articles for article (PubMed ID: 23612255)

  • 1. De novo trisomy 20p characterized by array comparative genomic hybridization: report of a novel case and review of the literature.
    Bartolini L; Sartori S; Lenzini E; Rigon C; Cainelli E; Agrati C; Toldo I; Donà M; Trevisson E
    Gene; 2013 Jul; 524(2):368-72. PubMed ID: 23612255
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A de novo 8q22.2-24.3 duplication in a patient with mild phenotype.
    Concolino D; Iembo MA; Moricca MT; Rapsomaniki M; Marotta R; Galesi O; Fichera M; Romano C; Strisciuglio P
    Eur J Med Genet; 2012 Jan; 55(1):67-70. PubMed ID: 21971480
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Partial trisomy due to a de novo duplication 22q11.1-22q13.1: a cat-eye syndrome variant with brain anomalies.
    Karcaaltincaba D; Ceylaner S; Ceylaner G; Dalkilic S; Karli-Oguz K; Kandemir O
    Genet Couns; 2010; 21(1):19-24. PubMed ID: 20420025
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De novo trisomy 20p of paternal origin.
    Chaabouni M; Turleau C; Karboul L; Jemaa LB; Maazoul F; Attié-Bitach T; Romana S; Chaabouni H
    Am J Med Genet A; 2007 May; 143A(10):1100-3. PubMed ID: 17431912
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization.
    Freitas ÉL; Gribble SM; Simioni M; Vieira TP; Silva-Grecco RL; Balarin MA; Prigmore E; Krepischi-Santos AC; Rosenberg C; Szuhai K; van Haeringen A; Carter NP; Gil-da-Silva-Lopes VL
    Am J Med Genet A; 2011 Nov; 155A(11):2754-61. PubMed ID: 21948691
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism.
    Eyüpoğlu FC; Sünnetçi D; Cine N; Savli H; Okten A; Açikgöz EG; Sönmez FM
    Genet Couns; 2014; 25(3):305-13. PubMed ID: 25365853
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A rare case of trisomy 11q23.3-11q25 and trisomy 22q11.1-22q11.21.
    Zou PS; Li HF; Chen LS; Ma M; Chen XH; Xue D; Cao DH
    Genet Mol Res; 2016 May; 15(2):. PubMed ID: 27173335
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Partial trisomy 3p and partial monosomy 11q associated with atrial septal defect, cleft palate, and developmental delay: a case report.
    Tan EC; Lim E; Cham B; Knight L; Ng I
    Cytogenet Genome Res; 2011; 134(4):319-24. PubMed ID: 21654159
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Complex rearrangement involving 9p deletion and duplication in a syndromic patient: genotype/phenotype correlation and review of the literature.
    Recalcati MP; Bellini M; Norsa L; Ballarati L; Caselli R; Russo S; Larizza L; Giardino D
    Gene; 2012 Jul; 502(1):40-5. PubMed ID: 22537675
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new case of pure partial 7q duplication.
    Alfonsi M; Palka C; Morizio E; Gatta V; Franchi S; Guanciali Franchi P; Zori R; Calabrese G; Palka G; Chiarelli F
    Cytogenet Genome Res; 2012; 136(1):1-5. PubMed ID: 22086126
    [TBL] [Abstract][Full Text] [Related]  

  • 14.
    Choi J; Yoon SY; Park BG; Eun BL; Kim M; Kwon JA
    Ann Lab Med; 2020 May; 40(3):277-280. PubMed ID: 31858772
    [No Abstract]   [Full Text] [Related]  

  • 15. Molecular karyotyping of an isolated partial trisomy 11q patient with additional findings.
    Kayhan G; Cavdarli B; Yirmibes Karaoguz M; Percin EF; Oztürk Kaymak A; Biri A; Ergun MA
    Gene; 2013 Jul; 524(2):355-60. PubMed ID: 23644025
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Another rare case of a child with de novo terminal 9p deletion and co-existing interstitial 9p duplication: clinical findings and molecular cytogenetic study by array-CGH.
    Kowalczyk M; Tomaszewska A; Podbioł-Palenta A; Constantinou M; Wawrzkiewicz-Witkowska A; Kowalski J; Kałużewski B; Zajączek S; Srebniak MI
    Cytogenet Genome Res; 2013; 139(1):9-16. PubMed ID: 22965227
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Array-CGH study of partial trisomy 9p without mental retardation.
    Bouhjar IB; Hannachi H; Zerelli SM; Labalme A; Gmidène A; Soyah N; Missaoui S; Sanlaville D; Elghezal H; Saad A
    Am J Med Genet A; 2011 Jul; 155A(7):1735-9. PubMed ID: 21626676
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Report of a patient with a trisomy of chromosome region 20q11.2-->20q12 and characterization with FISH.
    Wanderley HY; Schrander-Stumpel CT; Visser MO; Van Maanen-Op Het Roodt EA; Loneus WH; Engelen JJ
    Genet Couns; 2005; 16(3):277-82. PubMed ID: 16259325
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception.
    Serra G; Antona V; Cimador M; Collodoro G; Guida M; Piro E; Schierz IAM; Verde V; Giuffrè M; Corsello G
    Ital J Pediatr; 2023 Feb; 49(1):17. PubMed ID: 36759911
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A family with an inverted tandem duplication 5q22.1q23.2.
    Schmidt T; Bartels I; Liehr T; Burfeind P; Zoll B; Shoukier M
    Cytogenet Genome Res; 2013; 139(1):65-70. PubMed ID: 23051634
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.