Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Patricia, Smerdka"'
Autor:
Ulrike Schöck, Cornelia Blank, Patricia Smerdka, Max Wüstemann, Tilo Burkhardt, Bernt Schulze, Yadhu Kumar, Sabine Langer-Freitag, Michael Entezami, Roland Zimmermann, Gisela Raabe-Meyer, Maja Hempel, E. Ostermayer, Tina Schleicher, Wera Hofmann, Bernd Weil, Markus Schelling, Sebastian Grömminger, Markus Stumm, Karsten Haug
Publikováno v:
Prenatal Diagnosis. 34:185-191
Objective The objective of this study is to validate the diagnostic accuracy of a non-invasive prenatal test for detecting trisomies 13, 18, and 21 for a population in Germany and Switzerland. Methods Random massively parallel sequencing was applied
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b3aef9d7103846c5ce52e467009d5ce
https://doi.org/10.1002/pd.4278
https://doi.org/10.1002/pd.4278
Autor:
Ulrike Schöck, Sanli Erkan, Sándor Nagy, Wera Hofmann, Markus Stumm, Sebastian Grömminger, Mathias Ehrich, Joachim Bonnet, Rolf-Dieter Wegner, Patricia Smerdka, Erbil Yagmur
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 3, Iss 3, Pp 679-692 (2014)
Journal of Clinical Medicine, Vol 3, Iss 3, Pp 679-692 (2014)
Non-invasive prenatal testing (NIPT) by random massively parallel sequencing of maternal plasma DNA for multiple pregnancies is a promising new option for prenatal care since conventional non-invasive screening for fetal trisomies 21, 18 and 13 has l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcc11afd3ba95a30977e8e7fe57e019e
https://pubmed.ncbi.nlm.nih.gov/26237471
https://pubmed.ncbi.nlm.nih.gov/26237471
Autor:
Markus, Stumm, Michael, Entezami, Karsten, Haug, Cornelia, Blank, Max, Wüstemann, Bernt, Schulze, Gisela, Raabe-Meyer, Maja, Hempel, Markus, Schelling, Eva, Ostermayer, Sabine, Langer-Freitag, Tilo, Burkhardt, Roland, Zimmermann, Tina, Schleicher, Bernd, Weil, Ulrike, Schöck, Patricia, Smerdka, Sebastian, Grömminger, Yadhu, Kumar, Wera, Hofmann
Publikováno v:
Prenatal diagnosis. 34(2)
The objective of this study is to validate the diagnostic accuracy of a non-invasive prenatal test for detecting trisomies 13, 18, and 21 for a population in Germany and Switzerland.Random massively parallel sequencing was applied using Illumina sequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ff60e742896c6ce9012c6cec606f4e72
https://pubmed.ncbi.nlm.nih.gov/24222400
https://pubmed.ncbi.nlm.nih.gov/24222400
Autor:
Sebastian Grömminger, Ulrike Schöck, Sándor Nagy, Mathias Ehrich, Rolf-Dieter Wegner, Sanli Erkan, Joachim Bonnet, Markus Stumm, Patricia Smerdka, Erbil Yagmur, Wera Hofmann
Publikováno v:
Journal of Clinical Medicine, Vol 3, Iss 4, Pp 1333-1334 (2014)
Journal of Clinical Medicine
Journal of Clinical Medicine
The authors wish to make the following corrections to this paper [1]: On page 683 at the end of Section 3.2. lines 13–14, the word “no” is missing. The correct sentence should be: “There has been no evidence of false-negative NIPT results so
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7010edbce14a1c6f0c4a5aa8597cc65
http://www.mdpi.com/2077-0383/3/4/1333
http://www.mdpi.com/2077-0383/3/4/1333