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 *

223 related articles for article (PubMed ID: 30326779)

  • 61. Fluorescence in situ hybridization in uncultured amniocytes for detection of aneuploidy in 4210 prenatal cases.
    Jia CW; Wang SY; Ma YM; Lan YL; Si YM; Yu L; Zhou LY
    Chin Med J (Engl); 2011 Apr; 124(8):1164-8. PubMed ID: 21542989
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization on uncultured amniotic cells: experience with 630 samples.
    Mercier S; Bresson JL
    Ann Genet; 1995; 38(3):151-7. PubMed ID: 8540686
    [TBL] [Abstract][Full Text] [Related]  

  • 63. The Prenatal Diagnosis of Seven Fetuses with 7q11.23 Microdeletion or Microduplication.
    Dang Y; Wan S; Zheng Y; Song T; Li C; Li Y; Zhang J
    Fetal Pediatr Pathol; 2020 Aug; 39(4):269-276. PubMed ID: 31402733
    [No Abstract]   [Full Text] [Related]  

  • 64. [Application of Chromosomal Microarray Analysis for Chromosomal Abnormalities of Spontaneously Aborted Fetuses].
    Hu T; Zhu HM; Zhang Z; Wang JM; Zhang HX; Du Z; Li LP; Wang H; Liu SL
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2017 Sep; 48(5):732-735. PubMed ID: 29130666
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Application of chromosome microarray analysis in prenatal diagnosis.
    Xia M; Yang X; Fu J; Teng Z; Lv Y; Yu L
    BMC Pregnancy Childbirth; 2020 Nov; 20(1):696. PubMed ID: 33198662
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Experience using a rapid assay for aneuploidy and microdeletion/microduplication detection in over 2,900 prenatal specimens.
    Rosenfeld JA; Morton SA; Hummel C; Sulpizio SG; McDaniel LD; Schultz RA; Torchia BS; Ravnan JB; Ellison JW; Fisher AJ
    Fetal Diagn Ther; 2014; 36(3):231-41. PubMed ID: 25115231
    [TBL] [Abstract][Full Text] [Related]  

  • 67. [Application of chromosomal microarray analysis for fetuses with ventricular septal defects].
    Deng Q; Fu F; Li R; Jing X; Lei T; Yang X; Pan M; Zhen L; Han J; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):699-704. PubMed ID: 28981937
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Prenatal diagnosis by rapid aneuploidy detection and karyotyping: a prospective study of the role of ultrasound in 1589 second-trimester amniocenteses.
    Leung WC; Waters JJ; Chitty L
    Prenat Diagn; 2004 Oct; 24(10):790-5. PubMed ID: 15503279
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA).
    Hochstenbach R; Meijer J; van de Brug J; Vossebeld-Hoff I; Jansen R; van der Luijt RB; Sinke RJ; Page-Christiaens GC; Ploos van Amstel JK; de Pater JM
    Prenat Diagn; 2005 Nov; 25(11):1032-9. PubMed ID: 16231311
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Use of a DNA method, QF-PCR, in the prenatal diagnosis of fetal aneuploidies.
    Langlois S; Duncan A; ;
    J Obstet Gynaecol Can; 2011 Sep; 33(9):955-960. PubMed ID: 21923994
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Rapid prenatal diagnosis of aneuploidy from uncultured amniotic fluid cells using five-colour fluorescence in situ hybridization.
    Divane A; Carter NP; Spathas DH; Ferguson-Smith MA
    Prenat Diagn; 1994 Nov; 14(11):1061-9. PubMed ID: 7877954
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH).
    Witters I; Devriendt K; Legius E; Matthijs G; Van Schoubroeck D; Van Assche FA; Fryns JP
    Prenat Diagn; 2002 Jan; 22(1):29-33. PubMed ID: 11810646
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Rapid aneuploidy detection with multiplex ligation-dependent probe amplification: a prospective study of 4000 amniotic fluid samples.
    Van Opstal D; Boter M; de Jong D; van den Berg C; Brüggenwirth HT; Wildschut HI; de Klein A; Galjaard RJ
    Eur J Hum Genet; 2009 Jan; 17(1):112-21. PubMed ID: 18781187
    [TBL] [Abstract][Full Text] [Related]  

  • 74. [The value of non-invasive prenatal testing for the identification of fetal chromosome aneuploidies].
    Zhou Y; Wang Z; Mao Q; Shi D; Zhang L; Xu L; Li H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Nov; 36(11):1094-1096. PubMed ID: 31703133
    [TBL] [Abstract][Full Text] [Related]  

  • 75. [Application of fluorescence in situ hybridization to prenatal diagnosis of aneuploidy in 110 uncultured amniotic fluid samples].
    Liu H; Liao C; Huang YN; Pan M; Yi CX; Yuan SM; Hu SY; Zhong HZ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):453-6. PubMed ID: 20677157
    [TBL] [Abstract][Full Text] [Related]  

  • 76. [Molecular biology usefulness for rapid diagnosis of Down's syndrome and common aneuploidies].
    Fauret AL; Bilan F; Patri S; Couet D; Marechaud M; Pierre F; Gilbert-Dussardier B; Kitzis A
    Gynecol Obstet Fertil; 2009; 37(7-8):611-9. PubMed ID: 19574080
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Application of chromosome microarray analysis and karyotyping in diagnostic assessment of abnormal Down syndrome screening results.
    Kang H; Wang L; Li X; Gao C; Xie Y; Hu Y
    BMC Pregnancy Childbirth; 2022 Nov; 22(1):813. PubMed ID: 36333674
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Efficiency of expanded noninvasive prenatal testing in the detection of fetal subchromosomal microdeletion and microduplication in a cohort of 31,256 single pregnancies.
    Xue H; Yu A; Lin M; Chen X; Guo Q; Xu L; Huang H
    Sci Rep; 2022 Nov; 12(1):19750. PubMed ID: 36396840
    [TBL] [Abstract][Full Text] [Related]  

  • 79. [Rapid detection of the most common chromosomal aneuploidies in the second-trimester amniotic fluid using QF-PCR].
    Švecová I; Burjanivová T; Kršiaková J; Lasabová Z; Biringer K; Kapustová I; Móricová P; Danko J
    Ceska Gynekol; 2013 Aug; 78(4):373-8. PubMed ID: 24040987
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Prenatal diagnosis of fetuses with increased nuchal translucency using an approach based on quantitative fluorescent polymerase chain reaction and genomic microarray.
    Pan M; Han J; Zhen L; Yang X; Li R; Liao C; Li DZ
    Eur J Obstet Gynecol Reprod Biol; 2016 Feb; 197():164-7. PubMed ID: 26771907
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.