BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 20155755)

  • 1. A retrospective study by oligonucleotide array-CGH analysis in 50 fetuses with multiple malformations.
    Valduga M; Philippe C; Bach Segura P; Thiebaugeorges O; Miton A; Beri M; Bonnet C; Nemos C; Foliguet B; Jonveaux P
    Prenat Diagn; 2010 Apr; 30(4):333-41. PubMed ID: 20155755
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations.
    Le Caignec C; Boceno M; Saugier-Veber P; Jacquemont S; Joubert M; David A; Frebourg T; Rival JM
    J Med Genet; 2005 Feb; 42(2):121-8. PubMed ID: 15689449
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Array comparative genomic hybridization in prenatal diagnosis: another experience.
    Vialard F; Molina Gomes D; Leroy B; Quarello E; Escalona A; Le Sciellour C; Serazin V; Roume J; Ville Y; de Mazancourt P; Selva J
    Fetal Diagn Ther; 2009; 25(2):277-84. PubMed ID: 19521095
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies.
    Lee CN; Lin SY; Lin CH; Shih JC; Lin TH; Su YN
    BJOG; 2012 Apr; 119(5):614-25. PubMed ID: 22313859
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated cases.
    Schluth-Bolard C; Delobel B; Sanlaville D; Boute O; Cuisset JM; Sukno S; Labalme A; Duban-Bedu B; Plessis G; Jaillard S; Dubourg C; Henry C; Lucas J; Odent S; Pasquier L; Copin H; Latour P; Cordier MP; Nadeau G; Till M; Edery P; Andrieux J
    Eur J Med Genet; 2009; 52(5):291-6. PubMed ID: 19505601
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.
    D'Amours G; Kibar Z; Mathonnet G; Fetni R; Tihy F; Désilets V; Nizard S; Michaud JL; Lemyre E
    Clin Genet; 2012 Feb; 81(2):128-41. PubMed ID: 21496010
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies.
    Edelmann L; Hirschhorn K
    Ann N Y Acad Sci; 2009 Jan; 1151():157-66. PubMed ID: 19154522
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Copy number imbalances detected with a BAC-based array comparative genomic hybridization platform in congenital diaphragmatic hernia fetuses.
    Machado IN; Heinrich JK; Barini R; Peralta CF
    Genet Mol Res; 2011 Feb; 10(1):261-7. PubMed ID: 21341218
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Interstitial deletion 6p22.3-p24.3 characterized by CGH array in a foetus with multiple malformations.
    Colmant C; Brisset S; Tachdjian G; Gautier V; Ftouki M; Laroudie M; Druart L; Frydman R; Picone O
    Prenat Diagn; 2009 Sep; 29(9):908-10. PubMed ID: 19530104
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. Efficacy of array comparative genomic hybridization in a fetus with an inherited apparently balanced translocation: A case report.
    Park JK; Lee JI; Jo HC; Shin JK; Lee SA; Lee JH; Paik WY
    J Obstet Gynaecol Res; 2008 Aug; 34(4 Pt 2):653-7. PubMed ID: 18840174
    [TBL] [Abstract][Full Text] [Related]  

  • 14. De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency.
    Law LW; Lau TK; Fung TY; Leung TY; Wang CC; Choy KW
    BJOG; 2009 Jan; 116(2):339-43. PubMed ID: 19018765
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 --> qter) and partial monosomy 6q(6q26 --> qter) by high-resolution array CGH.
    Choy KW; Chan LW; Tang MH; Ng LK; Leung TY; Lau TK
    J Matern Fetal Neonatal Med; 2009 Nov; 22(11):1014-20. PubMed ID: 19900039
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Clinical utility of array comparative genomic hybridisation in prenatal setting.
    Lovrecic L; Remec ZI; Volk M; Rudolf G; Writzl K; Peterlin B
    BMC Med Genet; 2016 Nov; 17(1):81. PubMed ID: 27846804
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Detection of cryptic copy number variations in a fetus with congenital heart disease by array-based comparative genomic hybridization].
    HU P; WANG Y; JI XQ; LIN Y; Li L; ZHOU XY; CHEN J; MA DY; CAO L; Xu Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):133-6. PubMed ID: 21462121
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The use of comparative genomic hybridization and fluorescent in situ hybridization in postmortem pathology investigation of congenital malformations.
    Goemaere N; Douben H; Van Opstal D; Wouters C; Tibboel D; de Krijger R; de Klein A
    Pediatr Dev Pathol; 2010; 13(2):85-94. PubMed ID: 19594201
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.