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 *

234 related articles for article (PubMed ID: 22875502)

  • 1. [Array-based comparative genomic hybridization detection of copy number variations in a fetus with hypoplastic left-heart syndrome].
    Wang Y; Ma DY; Yang YQ; Zhou J; Zhou XY; Ji XQ; Chen J; Cao L; Hu P; Xu ZF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):439-42. PubMed ID: 22875502
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. [Prenatal diagnosis of two fetuses with de novo small supernumerary markers by single nucleotide polymorphism array based comparative genomic hybridization].
    Ji XQ; Li L; Lin Y; Ma DY; Liu A; Zhang JJ; Cheng J; Zhou J; Hu P; Xu ZF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Oct; 29(5):510-4. PubMed ID: 23042383
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. [Genetic analysis of a supernumerary derivative chromosome 15].
    Wang F; Yang Y; Wang CZ; He XI
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Feb; 29(1):77-81. PubMed ID: 22311498
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Cytogenetic analysis of a complex chromosomal imbalance 14q+ in a fetus featuring multiple congenital defects].
    Li L; Zhou XY; Ji XQ; Yang YQ; Cao L; Zhou J; Liu A; Cheng J; Liu Y; Hu P; Xu ZF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Apr; 29(2):214-7. PubMed ID: 22487837
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Comparative genomic hybridization to detect variation in the copy number of large DNA segments.
    Holcomb IN; Trask BJ
    Cold Spring Harb Protoc; 2011 Nov; 2011(11):1323-33. PubMed ID: 22046040
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and molecular description of the prenatal diagnosis of a fetus with a maternally inherited microduplication 22q11.2 of 2.5 Mb.
    Christopoulou G; Sismani C; Sakellariou M; Saklamaki M; Athanassiou V; Velissariou V
    Gene; 2013 Sep; 527(2):694-7. PubMed ID: 23506827
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evaluation of the efficacy of constitutional array-based comparative genomic hybridization in the diagnosis of aneuploidy using genomic and amplified DNA.
    Tan NH; Palmer R; Wang R
    J Obstet Gynaecol Res; 2010 Feb; 36(1):19-26. PubMed ID: 20178523
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
    Chen CP; Su YN; Chern SR; Hsu CY; Tsai FJ; Wu PC; Lee CC; Chen YT; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2011 Mar; 50(1):67-73. PubMed ID: 21482378
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease.
    Yan Y; Wu Q; Zhang L; Wang X; Dan S; Deng D; Sun L; Yao L; Ma Y; Wang L
    Ultrasound Obstet Gynecol; 2014 Apr; 43(4):404-12. PubMed ID: 24323407
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction.
    Chen CP; Ko TM; Huang WC; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Pan CW; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Jun; 55(3):415-8. PubMed ID: 27343326
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Molecular diagnosis of children with unexplained intellectual disability/ developmental delay by array-CGH].
    He XY; Chen XC; Li R; Li P; Lu AM
    Zhongguo Dang Dai Er Ke Za Zhi; 2015 May; 17(5):459-63. PubMed ID: 26014695
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterisation of hairy cell leukaemia by tiling resolution array-based comparative genome hybridisation: a series of 13 cases and review of the literature.
    Nordgren A; Corcoran M; Sääf A; Bremer A; Kluin-Nelemans HC; Schoumans J; Grandér D
    Eur J Haematol; 2010 Jan; 84(1):17-25. PubMed ID: 19682064
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Dandy-walker syndrome and microdeletions on chromosome 7].
    Liao C; Fu F; Li R; Pan M; Yang X; Yi CX; Li J; Li DZ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Feb; 29(1):48-51. PubMed ID: 22311491
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Application of chromosomal microarray in the evaluation of abnormal prenatal findings.
    Yatsenko SA; Davis S; Hendrix NW; Surti U; Emery S; Canavan T; Speer P; Hill L; Clemens M; Rajkovic A
    Clin Genet; 2013 Jul; 84(1):47-54. PubMed ID: 23020214
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.