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Detection of 22q11.2 microduplication by cell‐free DNA screening and chromosomal microarray in fetus with multiple anomalies
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113800/ https://www.ncbi.nlm.nih.gov/pubmed/27194416 http://dx.doi.org/10.1002/uog.15965 |
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author | Wu, W.‐J. Ma, G.‐C. Lin, Y.‐S. Yeang, C.‐H. Ni, Y.‐H. Li, W.‐C. Tsai, H.‐D. Shur‐Fen Gau, S. Chen, M. |
author_facet | Wu, W.‐J. Ma, G.‐C. Lin, Y.‐S. Yeang, C.‐H. Ni, Y.‐H. Li, W.‐C. Tsai, H.‐D. Shur‐Fen Gau, S. Chen, M. |
author_sort | Wu, W.‐J. |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-5113800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51138002016-12-02 Detection of 22q11.2 microduplication by cell‐free DNA screening and chromosomal microarray in fetus with multiple anomalies Wu, W.‐J. Ma, G.‐C. Lin, Y.‐S. Yeang, C.‐H. Ni, Y.‐H. Li, W.‐C. Tsai, H.‐D. Shur‐Fen Gau, S. Chen, M. Ultrasound Obstet Gynecol Letters to the Editor John Wiley & Sons, Ltd 2016-09-13 2016-10 /pmc/articles/PMC5113800/ /pubmed/27194416 http://dx.doi.org/10.1002/uog.15965 Text en © 2016 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of the International Society of Ultrasound in Obstetrics and Gynecology. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Letters to the Editor Wu, W.‐J. Ma, G.‐C. Lin, Y.‐S. Yeang, C.‐H. Ni, Y.‐H. Li, W.‐C. Tsai, H.‐D. Shur‐Fen Gau, S. Chen, M. Detection of 22q11.2 microduplication by cell‐free DNA screening and chromosomal microarray in fetus with multiple anomalies |
title | Detection of 22q11.2 microduplication by cell‐free DNA screening and chromosomal microarray in fetus with multiple anomalies |
title_full | Detection of 22q11.2 microduplication by cell‐free DNA screening and chromosomal microarray in fetus with multiple anomalies |
title_fullStr | Detection of 22q11.2 microduplication by cell‐free DNA screening and chromosomal microarray in fetus with multiple anomalies |
title_full_unstemmed | Detection of 22q11.2 microduplication by cell‐free DNA screening and chromosomal microarray in fetus with multiple anomalies |
title_short | Detection of 22q11.2 microduplication by cell‐free DNA screening and chromosomal microarray in fetus with multiple anomalies |
title_sort | detection of 22q11.2 microduplication by cell‐free dna screening and chromosomal microarray in fetus with multiple anomalies |
topic | Letters to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113800/ https://www.ncbi.nlm.nih.gov/pubmed/27194416 http://dx.doi.org/10.1002/uog.15965 |
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