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 *

167 related articles for article (PubMed ID: 24459084)

  • 1. Molecular characterization of distal 4q duplication in two patients using oligonucleotide array-based comparative genomic hybridization (oaCGH) analysis.
    Thapa M; Asamoah A; Gowans GC; Platky KC; Barch MJ; Mouchrani P; Rajakaruna C; Hersh JH
    Am J Med Genet A; 2014 Apr; 164A(4):1069-74. PubMed ID: 24459084
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: study of two cases and review of the literature.
    Rossi MR; DiMaio MS; Xiang B; Lu K; Kaymakcalan H; Seashore M; Mahoney MJ; Li P
    Am J Med Genet A; 2009 Dec; 149A(12):2788-94. PubMed ID: 19921640
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Overdosage of Hand2 causes limb and heart defects in the human chromosomal disorder partial trisomy distal 4q.
    Tamura M; Hosoya M; Fujita M; Iida T; Amano T; Maeno A; Kataoka T; Otsuka T; Tanaka S; Tomizawa S; Shiroishi T
    Hum Mol Genet; 2013 Jun; 22(12):2471-81. PubMed ID: 23449628
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication.
    Horbinski C; Carter EM; Heard PL; Sathanoori M; Hu J; Vockley J; Gunn S; Hale DE; Surti U; Cody JD
    Am J Med Genet A; 2008 Nov; 146A(22):2898-904. PubMed ID: 18932219
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Partial duplication of chromosome 4q (q31, q35): Auriculo-acro-renal syndrome].
    Carrascosa Romero MC; García Mialdea O; Vidal Company A; Cabezas Tapia ME; Gonzálvez Piñera J
    An Pediatr (Barc); 2008 Apr; 68(4):361-4. PubMed ID: 18394381
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial tandem duplication of bands q31.1 to q32.3 on chromosome 4 with mild phenotypic effect.
    Goodman BK; Capone GT; Hennessey J; Thomas GH
    Am J Med Genet; 1997 Dec; 73(2):119-24. PubMed ID: 9409859
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
    El-Ruby M; Hemly NA; Zaki MS
    Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pure partial trisomy 4q syndrome in a child with der(9)ins(9;4)(q34.3;q26q35.2)mat.
    Topcu V; Ilgin-Ruhi H; Yurur-Kutlay N; Ekici C; Vicdan A; Tukun FA
    Genet Couns; 2014; 25(1):1-6. PubMed ID: 24783648
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.
    Machado IN; Heinrich JK; Campanhol C; Rodrigues-Peres RM; Oliveira FM; Barini R
    Genet Mol Res; 2010 Mar; 9(1):441-8. PubMed ID: 20391329
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Insertional translocation leading to a 4q13 duplication including the EPHA5 gene in two siblings with attention-deficit hyperactivity disorder.
    Matoso E; Melo JB; Ferreira SI; Jardim A; Castelo TM; Weise A; Carreira IM
    Am J Med Genet A; 2013 Aug; 161A(8):1923-8. PubMed ID: 23824631
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case.
    Tuğ E; Yirmibeş Karaoğuz M; Kayhan G; Ergün MA; Perçin FE
    Am J Med Genet A; 2014 Jul; 164A(7):1770-6. PubMed ID: 24677787
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Further contribution to the description of phenotypes associated with partial 4q duplication.
    Zollino M; Zampino G; Torrioli G; Pomponi MG; Neri G
    Am J Med Genet; 1995 May; 57(1):69-73. PubMed ID: 7645603
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genotype-phenotype analysis of 4q deletion syndrome: proposal of a critical region.
    Strehle EM; Yu L; Rosenfeld JA; Donkervoort S; Zhou Y; Chen TJ; Martinez JE; Fan YS; Barbouth D; Zhu H; Vaglio A; Smith R; Stevens CA; Curry CJ; Ladda RL; Fan ZJ; Fox JE; Martin JA; Abdel-Hamid HZ; McCracken EA; McGillivray BC; Masser-Frye D; Huang T
    Am J Med Genet A; 2012 Sep; 158A(9):2139-51. PubMed ID: 22847869
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Translocation/duplication of 9p onto a duplicated 4q.
    Rivera H; Figuera LE; Vasquez AI
    Genet Couns; 1992; 3(4):201-3. PubMed ID: 1472355
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: a genotype-phenotype analysis.
    Ronzoni L; Peron A; Bianchi V; Baccarin M; Guerneri S; Silipigni R; Lalatta F; Bedeschi MF
    Am J Med Genet A; 2015 Jul; 167(7):1551-9. PubMed ID: 25851921
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Instability of isochromosome 4p in a child with pure trisomy 4p syndrome features and entire 4q-arm translocation.
    Pota P; Grammatopoulou V; Torti E; Braddock S; Batanian JR
    Cytogenet Genome Res; 2014; 144(4):280-4. PubMed ID: 25632983
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Familial 9q22.3 microduplication spanning PTCH1 causes short stature syndrome with mild intellectual disability and dysmorphic features.
    Izumi K; Hahn A; Christ L; Curtis C; Neilson DE
    Am J Med Genet A; 2011 Jun; 155A(6):1384-9. PubMed ID: 21567912
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.