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Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods”
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575504/ https://www.ncbi.nlm.nih.gov/pubmed/28675625 http://dx.doi.org/10.1002/pd.5072 |
| _version_ | 1783260059964276736 |
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| author | Ryan, Allison Martin, Kimberly A. |
| author_facet | Ryan, Allison Martin, Kimberly A. |
| author_sort | Ryan, Allison |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-5575504 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2017 |
| publisher | John Wiley and Sons Inc. |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-55755042017-09-18 Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods” Ryan, Allison Martin, Kimberly A. Prenat Diagn Correspondence John Wiley and Sons Inc. 2017-07-03 2017-07 /pmc/articles/PMC5575504/ /pubmed/28675625 http://dx.doi.org/10.1002/pd.5072 Text en © 2017 Natera. Prenatal Diagnosis published by John Wiley & Sons, Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
| spellingShingle | Correspondence Ryan, Allison Martin, Kimberly A. Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods” |
| title | Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods” |
| title_full | Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods” |
| title_fullStr | Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods” |
| title_full_unstemmed | Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods” |
| title_short | Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods” |
| title_sort | comment on “noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods” |
| topic | Correspondence |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575504/ https://www.ncbi.nlm.nih.gov/pubmed/28675625 http://dx.doi.org/10.1002/pd.5072 |
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