BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

248 related articles for article (PubMed ID: 24444558)

  • 1. [Prenatal diagnosis of 22q11.2 microdeletion by multiplex ligation-dependent probe amplification].
    Luo CY; Ma DY; Zhang JJ; Hu P; Cao L; Ji XQ; Zhou J; Liu A; Wu Y; Cheng J; Lin Y; Xu ZF
    Zhonghua Fu Chan Ke Za Zhi; 2013 Nov; 48(11):824-7. PubMed ID: 24444558
    [TBL] [Abstract][Full Text] [Related]  

  • 2. MLPA: a prenatal diagnostic tool for the study of congenital heart defects?
    Mademont-Soler I; Morales C; Soler A; Clusellas N; Margarit E; Martínez-Barrios E; Martínez JM; Sánchez A
    Gene; 2012 May; 500(1):151-4. PubMed ID: 22446045
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
    Kuo YL; Chen CP; Wang LK; Ko TM; Chang TY; Chern SR; Wu PS; Chen YT; Chang SY
    Taiwan J Obstet Gynecol; 2014 Jun; 53(2):248-51. PubMed ID: 25017279
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Incidences of micro-deletion/duplication 22q11.2 detected by multiplex ligation-dependent probe amplification in patients with congenital cardiac disease who are scheduled for cardiac surgery.
    Hu Y; Zhu X; Yang Y; Mo X; Sheng M; Yao J; Wang D
    Cardiol Young; 2009 Apr; 19(2):179-84. PubMed ID: 19224675
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Clinical detection of 22q11 microdeletion in the patients with congenital heart disease by multiplex ligation dependent probe amplification].
    Chen Y; Kan HJ; Mao J; Ding J; Meng QX; Li HB; Cheng HB; Liu MJ; Sun Y; Yan WH; Li H
    Zhonghua Er Ke Za Zhi; 2011 Apr; 49(4):316-9. PubMed ID: 21624212
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with Wolf-Hirschhorn syndrome.
    Yang WX; Pan H; Wang ST; Li L; Wu HR; Qi Y
    Taiwan J Obstet Gynecol; 2016 Feb; 55(1):104-8. PubMed ID: 26927259
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rapid detection of aneuploidy and unbalanced chromosomal rearrangements by subtelomeric multiplex ligation-dependent probe amplification in fetuses with congenital heart disease.
    Wang J; Liu Z; Liu H; Li N; Li S; Chen X; Lin Y; Wang H; Zhu J; Liu S
    Fetal Diagn Ther; 2013; 34(2):110-5. PubMed ID: 23774328
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Microdeletion of 22q11 and conotruncal cardiopathies: contribution of prenatal diagnosis].
    Verspyck E; Joly G; Rossi A; David N; Blaysat G; Henocq A; Moirot H; Labadie G; Marpeau L
    J Gynecol Obstet Biol Reprod (Paris); 1999 Oct; 28(6):534-7. PubMed ID: 10598346
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.
    Zhang X; Xu Y; Liu D; Geng J; Chen S; Jiang Z; Fu Q; Sun K
    BMC Genomics; 2015 May; 16(1):364. PubMed ID: 25952753
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Combined G-banded karyotyping and multiplex ligation-dependent probe amplification for the detection of chromosomal abnormalities in fetuses with congenital heart defects].
    Liu Y; Xie J; Geng Q; Xu Z; Wu W; Luo F; Li S; Wang Q; Chen W; Tan H; Zhang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):1-5. PubMed ID: 28186583
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
    Chen M; Hwu WL; Kuo SJ; Chen CP; Yin PL; Chang SP; Lee DJ; Chen TH; Wang BT; Lin CC
    Ultrasound Obstet Gynecol; 2006 Dec; 28(7):939-43. PubMed ID: 17121426
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Testing for 22q11 microdeletion in 146 fetuses with nuchal translucency above the 99th percentile and a normal karyotype.
    Lautrup CK; Kjaergaard S; Brøndum-Nielsen K; Fagerberg C; Hertz JM; Petersen OB; Jørgensen MW; Vogel I
    Acta Obstet Gynecol Scand; 2008; 87(11):1252-5. PubMed ID: 18951212
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Diagnosis of 22q11 deletion and duplication in congenital heart disease by multiplex ligation dependent probe amplification].
    Yang YH; Hu YL; Zhu XY; Mo XM; Wang DJ; Yao JC; Sheng M; Zhu HY; Li J; Ru T; Wang ZQ
    Zhongguo Dang Dai Er Ke Za Zhi; 2009 Nov; 11(11):892-6. PubMed ID: 20113655
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Application of multiplex ligation-dependent probe amplification for rapid detection of aneuploidies and structural chromosomal abnormalities in prenatal diagnosis].
    Zhang J; Hu P; Luo C; Ji Q; Zhou J; Liu A; Ma D; Xu Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):11-5. PubMed ID: 24510553
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization.
    Chen M; Yang YS; Shih JC; Lin WH; Lee DJ; Lin YS; Chou CH; Cameron AD; Ginsberg NA; Chen CA; Lee ML; Ma GC
    Ultrasound Obstet Gynecol; 2014 Apr; 43(4):396-403. PubMed ID: 23828768
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital heart defects and chromosomal anomalies including 22q11 microdeletion (CATCH 22).
    Soares G; Alvares S; Rocha C; Teixeira MF; Mota MC; Reis MI; Feijó MJ; Lima MR; Pinto MR
    Rev Port Cardiol; 2005 Mar; 24(3):349-71. PubMed ID: 15929620
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Multiplex ligation-dependent probe amplification (MLPA): a reliable alternative for fetal chromosome analysis?
    Chitty LS; Kistler J; Akolekar R; Liddle S; Nicolaides K; Levett L
    J Matern Fetal Neonatal Med; 2012 Aug; 25(8):1383-6. PubMed ID: 22098527
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect.
    Zhang J; Ma D; Wang Y; Cao L; Wu Y; Qiao F; Liu A; Li L; Lin Y; Liu G; Liu C; Hu P; Xu Z
    Mol Cytogenet; 2015; 8():100. PubMed ID: 26715944
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.