Literature DB >> 26468773

Cell-Free DNA Testing for Fetal Chromosomal Anomalies in clinical practice: Austrian-German-Swiss Recommendations for non-invasive prenatal tests (NIPT).

M Schmid1, P Klaritsch2, W Arzt3, T Burkhardt4, H C Duba5, M Häusler2, E Hafner6, U Lang2, B Pertl7, M Speicher8, H Steiner9, S Tercanli10, E Merz11, K S Heling12, B Eiben13.   

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Year:  2015        PMID： 26468773     DOI： 10.1055/s-0035-1553804

Source DB:  PubMed          Journal:  Ultraschall Med        ISSN： 0172-4614            Impact factor:   6.548


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  3 in total

1.  Noninvasive Prenatal Testing for Trisomies 21, 18, and 13, Sex Chromosome Aneuploidies, and Microdeletions: A Health Technology Assessment.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2019-02-19

2.  Cell-free DNA Testing in Routine Practice: Characterisation of a Cohort with Positive Results for Trisomies, Sex Chromosome Anomalies and Microdeletions.

Authors:  Ismail Tekesin
Journal:  Geburtshilfe Frauenheilkd       Date:  2020-11-24       Impact factor: 2.915

3.  Analysis of cell-free DNA in a consecutive series of 13,607 routine cases for the detection of fetal chromosomal aneuploidies in a single center in Germany.

Authors:  Heike Borth; Anna Teubert; Ralf Glaubitz; Sarah Knippenberg; Nargül Kutur; Thomas Winkler; Bernd Eiben
Journal:  Arch Gynecol Obstet       Date:  2020-11-05       Impact factor: 2.344
  3 in total

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