These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

124 related articles for article (PubMed ID: 12244548)

  • 1. 20-Mb duplication of chromosome 9p in a girl with minimal physical findings and normal IQ: narrowing of the 9p duplication critical region to 6 Mb.
    Bonaglia MC; Giorda R; Carrozzo R; Roncoroni ME; Grasso R; Borgatti R; Zuffardi O
    Am J Med Genet; 2002 Oct; 112(2):154-9. PubMed ID: 12244548
    [TBL] [Abstract][Full Text] [Related]  

  • 2. FISH analysis in detecting 9p duplication (p22p24).
    Guanciali Franchi P; Calabrese G; Morizio E; Modestini E; Stuppia L; Mingarelli R; Palka G
    Am J Med Genet; 2000 Jan; 90(1):35-7. PubMed ID: 10602115
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Direct duplication of 9p22-->p24 in a child with duplication 9p syndrome.
    Fujimoto A; Lin MS; Schwartz S
    Am J Med Genet; 1998 May; 77(4):268-71. PubMed ID: 9600733
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Inverted duplications are recurrent rearrangements always associated with a distal deletion: description of a new case involving 2q.
    Bonaglia MC; Giorda R; Poggi G; Raggi ME; Rossi E; Baroncini A; Giglio S; Borgatti R; Zuffardi O
    Eur J Hum Genet; 2000 Aug; 8(8):597-603. PubMed ID: 10951522
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Chromosome 7q22-q31 duplication: report of a new case and review.
    Mégarbané A; Gosset P; Souraty N; Lapierre JM; Turleau C; Vekemans M; Loiselet J; Prieur M
    Am J Med Genet; 2000 Nov; 95(2):164-8. PubMed ID: 11078569
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy.
    Wyandt HE; Lebo RV; Fenerci EY; Sadhu DN; Milunsky JM
    Am J Med Genet; 2000 Aug; 93(4):305-12. PubMed ID: 10946358
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Duplication of 9 p11.2-p13.1: a benign cytogenetic variant.
    Di Giacomo MC; Cesarano C; Bukvic N; Manisali E; Guanti G; Susca F
    Prenat Diagn; 2004 Aug; 24(8):619-22. PubMed ID: 15305349
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Delineation of a duplication map of chromosome 3q: a new case confirms the exclusion of 3q25-q26.2 from the duplication 3q syndrome critical region.
    Rizzu P; Haddad BR; Vallcorba I; Alonso A; Ferro MT; Garcia-Sagredo JM; Baldini A
    Am J Med Genet; 1997 Feb; 68(4):428-32. PubMed ID: 9021016
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Duplication of segment 1p21 following paternal insertional translocation, ins(6;1)(q25;p13.3p22.1).
    Utkus A; Sorokina I; Kucinskas V; Röthlisberger B; Balmer D; Brecevic L; Schinzel A
    J Med Genet; 1999 Jan; 36(1):73-6. PubMed ID: 9950373
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH.
    Barber JC; Maloney VK; Huang S; Bunyan DJ; Cresswell L; Kinning E; Benson A; Cheetham T; Wyllie J; Lynch SA; Zwolinski S; Prescott L; Crow Y; Morgan R; Hobson E
    Eur J Hum Genet; 2008 Jan; 16(1):18-27. PubMed ID: 17940555
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndrome.
    Girirajan S; Williams S; Garbern J; Nowak N; Hatchwell E; Elsea S
    Clin Genet; 2007 Jul; 72(1):47-58. PubMed ID: 17594399
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A case of 9p-syndrome identified chromosome 20 on chromosome 9p by M-FISH].
    Koseki N; Obara Y; Ookawa A; Katsumi M; Funato T; Kaku M
    Rinsho Byori; 2001 Oct; 49(10):1045-8. PubMed ID: 11769470
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Delimitation of duplicated segments and identification of their parental origin in two partial chromosome 3p duplications.
    Antonini S; Kim CA; Sugayama SM; Vianna-Morgante AM
    Am J Med Genet; 2002 Nov; 113(2):144-50. PubMed ID: 12407704
    [TBL] [Abstract][Full Text] [Related]  

  • 16. FISH mapping of the sex-reversal region on human chromosome 9p in two XY females and in primates.
    Shan Z; Zabel B; Trautmann U; Hillig U; Ottolenghi C; Wan Y; Haaf T
    Eur J Hum Genet; 2000 Mar; 8(3):167-73. PubMed ID: 10780781
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Boy with seizures (West syndrome) and distal 7q duplication syndrome due to an unbalanced 7q;9p translocation.
    Tüysüz B; Demirel A; Uysal S; Beyer V; Bartsch O
    Genet Couns; 2008; 19(1):29-35. PubMed ID: 18564498
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis.
    Bartsch O; Vlcková Z; Erdogan F; Ullmann R; Novotná D; Spiegel M; Beyer V; Haaf T; Zechner U; Seemanová E
    Cytogenet Genome Res; 2007; 119(1-2):158-64. PubMed ID: 18160797
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genitourinary phenotype in XX patients with distal 9p monosomy.
    Fujimoto Y; Okuyama T; Iijima M; Tanaka T; Horikawa R; Yamada K; Ogata T
    Mol Genet Metab; 2004 Jun; 82(2):173-9. PubMed ID: 15172006
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11.
    Hu J; Sathanoori M; Kochmar S; Madan-Khetarpal S; McGuire M; Surti U
    Am J Med Genet A; 2013 Jan; 161A(1):179-84. PubMed ID: 23225375
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.