Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Bernd Weil"'
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:
Stefan Wiemann, Brigitte Obermaier, Stefan Bauersachs, Bernd Weil, Bernhard Korn, Michael Böcher, Michaela Klein, Wilhelm Ansorge, Dagmar Heubner, Hans-Werner Mewes, Sabine Glassl, Jürgen Lauber, Birgit Ottenwälder, Karl Köhrer, R. Wambutt, Andreas Beyer, Ruth Wellenreuther, Helmut Blum, A. Düsterhöft, Jens Tampe, Johannes Gassenhuber, Helmut Blöcker, Normann Strack, Annemarie Poustka
Publikováno v:
Genome Research. 11:422-435
With the complete human genomic sequence being unraveled, the focus will shift to gene identification and to the functional analysis of gene products. The generation of a set of cDNAs, both sequences and physical clones, which contains the complete a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::419dfdcdab4b8c5e47faa389a77dd1f4
https://doi.org/10.1101/gr.154701
https://doi.org/10.1101/gr.154701
Publikováno v:
Gene. 216:267-276
DmX is a novel gene from Drosophila melanogaster located on the X chromosome in region 5D5/6-E1. The molecular analysis of the genomic and cDNA sequences of DmX shows that the gene spans appr. 16kb and displays a mosaic structure with 15 exons. The 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72d770234eed6f813c9754828b35fdc2
https://doi.org/10.1016/s0378-1119(98)00347-3
https://doi.org/10.1016/s0378-1119(98)00347-3
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
Publikováno v:
Erwachsenenbildung : Vierteljahresschrift für Theorie und Praxis
Männerbildung
Männerbildung
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1a54ccf821ad20adffc7fb2b991380d5
https://www.ssoar.info/ssoar/handle/document/64270
https://www.ssoar.info/ssoar/handle/document/64270
