BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

325 related articles for article (PubMed ID: 20376795)

  • 21. 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]  

  • 22. Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
    Simovich MJ; Yatsenko SA; Kang SH; Cheung SW; Dudek ME; Pursley A; Ward PA; Patel A; Lupski JR
    Prenat Diagn; 2007 Dec; 27(12):1112-7. PubMed ID: 17849500
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
    Peeters H; Vermeesch J; Fryns JP
    Genet Couns; 2008; 19(4):365-71. PubMed ID: 19239079
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
    Tan YQ; Di YF; Song YZ; Cheng DH; Li LY; Lu GX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):392-6. PubMed ID: 17680527
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Periventricular heterotopia in a boy with interstitial deletion of chromosome 4p.
    Gawlik-Kuklinska K; Wierzba J; Wozniak A; Iliszko M; Debiec-Rychter M; Dubaniewicz-Wybieralska M; Limon J
    Eur J Med Genet; 2008; 51(2):165-71. PubMed ID: 18243084
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features.
    Haddad MR; Mignon-Ravix C; Cacciagli P; Mégarbané A; Villard L
    Eur J Med Genet; 2009; 52(4):211-7. PubMed ID: 19379847
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.
    Brenk CH; Prott EC; Trost D; Hoischen A; Walldorf C; Radlwimmer B; Wieczorek D; Propping P; Gillessen-Kaesbach G; Weber RG; Engels H
    Eur J Hum Genet; 2007 Jan; 15(1):35-44. PubMed ID: 17024214
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
    Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W
    Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
    Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
    Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection.
    Delatycki MB; Voullaire L; Francis D; Petrovic V; Robertson A; Webber LM; Slater HR
    J Med Genet; 1999 Apr; 36(4):335-8. PubMed ID: 10227406
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Identification and molecular characterization of two novel chromosomal deletions associated with autism.
    Chien WH; Gau SS; Wu YY; Huang YS; Fang JS; Chen YJ; Soong WT; Chiu YN; Chen CH
    Clin Genet; 2010 Nov; 78(5):449-56. PubMed ID: 20236125
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [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]  

  • 34. Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).
    Schoumans J; Ruivenkamp C; Holmberg E; Kyllerman M; Anderlid BM; Nordenskjöld M
    J Med Genet; 2005 Sep; 42(9):699-705. PubMed ID: 16141005
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS; Kamel AK; Helmy NA
    Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
    [TBL] [Abstract][Full Text] [Related]  

  • 36. De novo unbalanced translocation 2;4 characterized by metaphase CGH and array CGH in a child with mental retardation and dysmorphic features.
    Debost-Legrand A; Capri Y; Gouas L; Pebrel-Richard C; Veronese L; Tchirkov A; Haoud K; Boespflug-Tanguy O; Goumy C; Vago P
    Pathol Biol (Paris); 2011 Dec; 59(6):309-13. PubMed ID: 21145667
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A PATIENT WITH PARTIAL CHROMOSOME 12q DUPLICATION AND 10q DELETION.
    Saat H; Soysal Y; Kurtgoz S; Ergun MA; Percin EF
    Genet Couns; 2015; 26(4):401-7. PubMed ID: 26852510
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Unbalanced translocation in an adult patient with premature ovarian failure and mental retardation detected by spectral karyotyping and array-comparative genomic hybridization.
    Guo QS; Qin SY; Zhou SF; He L; Ma D; Zhang YP; Xiong Y; Peng T; Cheng Y; Li XT
    Eur J Clin Invest; 2009 Aug; 39(8):729-37. PubMed ID: 19515099
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A subtle familial translocation t(3;21)(p26.3;q22.3): an apparently healthy boy with a 3p deletion and 21q duplication.
    Gijsbers AC; van Haeringen A; Bosch CA; Hansson K; Verschuren M; Bakker E; Breuning MH; Ruivenkamp CA
    Cytogenet Genome Res; 2010 Jun; 128(4):245-9. PubMed ID: 20431279
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cytogenetic and molecular analysis in trisomy 12p.
    Allen TL; Brothman AR; Carey JC; Chance PF
    Am J Med Genet; 1996 May; 63(1):250-6. PubMed ID: 8723118
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.