BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

290 related articles for article (PubMed ID: 22086062)

  • 21. ACOG Committee Opinion No. 446: array comparative genomic hybridization in prenatal diagnosis.
    Obstet Gynecol; 2009 Nov; 114(5):1161-1163. PubMed ID: 20168129
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Applications of array comparative genomic hybridization in obstetrics.
    Fruhman G; Van den Veyver IB
    Obstet Gynecol Clin North Am; 2010 Mar; 37(1):71-85, Table of Contents. PubMed ID: 20494259
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Applied research of combined G-banding and array-CGH in the prenatal diagnosis of ultrasonographic abnormalities in fetuses].
    Fu W; Lu J; Xu L; Zheng L; Zhang Y; Zhong Y; Wang Y; Jin Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):737-42. PubMed ID: 25449078
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. [Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities].
    ten Kate LP
    Ned Tijdschr Geneeskd; 2006 Jul; 150(29):1608-12. PubMed ID: 16901063
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Karyotype versus genomic hybridization for the prenatal diagnosis of chromosomal abnormalities: a metaanalysis.
    Saldarriaga W; García-Perdomo HA; Arango-Pineda J; Fonseca J
    Am J Obstet Gynecol; 2015 Mar; 212(3):330.e1-10. PubMed ID: 25305409
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 0.5 Mb array as a first-line prenatal cytogenetic test in cases without ultrasound abnormalities and its implementation in clinical practice.
    Srebniak MI; Mout L; Van Opstal D; Galjaard RJ
    Hum Mutat; 2013 Sep; 34(9):1298-303. PubMed ID: 23674485
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong.
    Kan AS; Lau ET; Tang WF; Chan SS; Ding SC; Chan KY; Lee CP; Hui PW; Chung BH; Leung KY; Ma T; Leung WC; Tang MH
    PLoS One; 2014; 9(2):e87988. PubMed ID: 24505343
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. [Prenatal diagnosis for a women with a suspected birth history of Angelman syndrome].
    Guo C; Xiao J; Wang J; Yang L; Tang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):827-9. PubMed ID: 26663058
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Holoprosencephaly: An update on cytogenetic abnormalities.
    Bendavid C; Dupé V; Rochard L; Gicquel I; Dubourg C; David V
    Am J Med Genet C Semin Med Genet; 2010 Feb; 154C(1):86-92. PubMed ID: 20104602
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Application of chromosomal karyotyping analysis and array CGH for fetal abnormalities detected by ultrasonography].
    Wang Y; Tang B; Guo L; Chen H; Lu J; Yin A
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug; 34(4):550-553. PubMed ID: 28777857
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?
    Ganesamoorthy D; Bruno DL; McGillivray G; Norris F; White SM; Adroub S; Amor DJ; Yeung A; Oertel R; Pertile MD; Ngo C; Arvaj AR; Walker S; Charan P; Palma-Dias R; Woodrow N; Slater HR
    BJOG; 2013 Apr; 120(5):594-606. PubMed ID: 23332022
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Cytogenetics in reproductive medicine: the contribution of comparative genomic hybridization (CGH).
    Wells D; Levy B
    Bioessays; 2003 Mar; 25(3):289-300. PubMed ID: 12596234
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal diagnosis by array-CGH.
    Rickman L; Fiegler H; Carter NP; Bobrow M
    Eur J Med Genet; 2005; 48(3):232-40. PubMed ID: 16179219
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal diagnosis by array-based comparative genomic hybridization in the clinical laboratory setting.
    Breman AM; Bi WM; Cheung SW
    Beijing Da Xue Xue Bao Yi Xue Ban; 2009 Aug; 41(4):500-4. PubMed ID: 19727248
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Application of a target array comparative genomic hybridization to prenatal diagnosis.
    Park JH; Woo JH; Shim SH; Yang SJ; Choi YM; Yang KS; Cha DH
    BMC Med Genet; 2010 Jun; 11():102. PubMed ID: 20576126
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.