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Detection of 22q11.2 microduplication by cell‐free DNA screening and chromosomal microarray in fetus with multiple anomalies

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2016
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.
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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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