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Volumn 1075, Issue , 2006, Pages 144-147

Detection of SNPs in the plasma of pregnant women and in the urine of kidney transplant recipients by mass spectrometry

Author keywords

Cell free DNA; Size fractionation; SNPs; Urinary DNA

Indexed keywords

DNA;

EID: 33749553552     PISSN: 00778923     EISSN: 17496632     Source Type: Book Series    
DOI: 10.1196/annals.1368.019     Document Type: Conference Paper
Times cited : (11)

References (9)
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    • Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma: Case report
    • LI, Y. et al. 2004. Improved prenatal detection of a fetal point mutation for achondroplasia by the use of size-fractionated circulatory DNA in maternal plasma: case report. Prenat. Diagn. 24: 896-898.
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    • LI, Y. et al. 2005. Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma. JAMA 293: 843-849.
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    • Presence of donor- and recipient-derived DNA in cell-free urine samples of renal transplantation recipients: Urinary DNA chimerism
    • ZHANG, J. et al. 1999. Presence of donor- and recipient-derived DNA in cell-free urine samples of renal transplantation recipients: urinary DNA chimerism. Clin. Chem. 45: 1741-1746.
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    • Cell-free DNA in urine: A marker for kidney graft rejection, but not for prenatal diagnosis?
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.