The fetal sequencing consortium: The value of multidisciplinary dialog and collaboration
Key points What is already known about this topic? Exome and genome sequencing is increasingly used in prenatal diagnosis. Clinicians face numerous challenges in how to interpret genes and variants identified through prenatal sequencing. What does this study add? An international, multidisciplinary...
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Veröffentlicht in: | Prenatal diagnosis 2022-06, Vol.42 (7), p.807-810 |
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container_title | Prenatal diagnosis |
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creator | Giordano, Jessica L. Wapner, Ronald J. |
description | Key points
What is already known about this topic?
Exome and genome sequencing is increasingly used in prenatal diagnosis. Clinicians face numerous challenges in how to interpret genes and variants identified through prenatal sequencing.
What does this study add?
An international, multidisciplinary consortium allows for real‐time collaboration on ongoing cases, assessment of new technologies, and the opportunity to create a novel fetal sequencing repository. |
doi_str_mv | 10.1002/pd.6190 |
format | Article |
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What is already known about this topic?
Exome and genome sequencing is increasingly used in prenatal diagnosis. Clinicians face numerous challenges in how to interpret genes and variants identified through prenatal sequencing.
What does this study add?
An international, multidisciplinary consortium allows for real‐time collaboration on ongoing cases, assessment of new technologies, and the opportunity to create a novel fetal sequencing repository.</description><identifier>ISSN: 0197-3851</identifier><identifier>EISSN: 1097-0223</identifier><identifier>DOI: 10.1002/pd.6190</identifier><identifier>PMID: 35661204</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Fetuses</subject><ispartof>Prenatal diagnosis, 2022-06, Vol.42 (7), p.807-810</ispartof><rights>2022 John Wiley & Sons Ltd.</rights><rights>This article is protected by copyright. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1900-b64f47faa0f273bef328242a127407e45b54996d4f19cbd8944b8740c4dd91cb3</citedby><cites>FETCH-LOGICAL-c1900-b64f47faa0f273bef328242a127407e45b54996d4f19cbd8944b8740c4dd91cb3</cites><orcidid>0000-0002-2265-0691</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpd.6190$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpd.6190$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35661204$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Giordano, Jessica L.</creatorcontrib><creatorcontrib>Wapner, Ronald J.</creatorcontrib><title>The fetal sequencing consortium: The value of multidisciplinary dialog and collaboration</title><title>Prenatal diagnosis</title><addtitle>Prenat Diagn</addtitle><description>Key points
What is already known about this topic?
Exome and genome sequencing is increasingly used in prenatal diagnosis. Clinicians face numerous challenges in how to interpret genes and variants identified through prenatal sequencing.
What does this study add?
An international, multidisciplinary consortium allows for real‐time collaboration on ongoing cases, assessment of new technologies, and the opportunity to create a novel fetal sequencing repository.</description><subject>Fetuses</subject><issn>0197-3851</issn><issn>1097-0223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kF1LwzAUhoMobk7xH0jBCwXpzFfTxjuZnzDQiwnelbRJZkba1KZV9u9N3fRC8OoEzpOX57wAHCM4RRDiy0ZOGeJwB4wR5GkMMSa7YAxReJMsQSNw4P0qgBnm6T4YkYQxhCEdg9fFm4q06oSNvHrvVV2aehmVrvau7UxfXUUD8CFsryKno6q3nZHGl6axphbtOpJGWLeMRC3DL2tF4VrRGVcfgj0trFdH2zkBL3e3i9lDPH-6f5xdz-My-MK4YFTTVAsBNU5JoTQJjhQLhFMKU0WTIqGcM0k14mUhM05pkYVVSaXkqCzIBJxvcpvWBX_f5VXQU8GkVq73OWYpSTjNEhjQ0z_oyvVtHewGimUZYYwE6mxDla3zvlU6b1pThVNzBPOh7LyR-VB2IE-2eX1RKfnL_bQbgIsN8GmsWv-Xkz_ffMd9Abu0hpc</recordid><startdate>202206</startdate><enddate>202206</enddate><creator>Giordano, Jessica L.</creator><creator>Wapner, Ronald J.</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2265-0691</orcidid></search><sort><creationdate>202206</creationdate><title>The fetal sequencing consortium: The value of multidisciplinary dialog and collaboration</title><author>Giordano, Jessica L. ; Wapner, Ronald J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1900-b64f47faa0f273bef328242a127407e45b54996d4f19cbd8944b8740c4dd91cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Fetuses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Giordano, Jessica L.</creatorcontrib><creatorcontrib>Wapner, Ronald J.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Prenatal diagnosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Giordano, Jessica L.</au><au>Wapner, Ronald J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The fetal sequencing consortium: The value of multidisciplinary dialog and collaboration</atitle><jtitle>Prenatal diagnosis</jtitle><addtitle>Prenat Diagn</addtitle><date>2022-06</date><risdate>2022</risdate><volume>42</volume><issue>7</issue><spage>807</spage><epage>810</epage><pages>807-810</pages><issn>0197-3851</issn><eissn>1097-0223</eissn><abstract>Key points
What is already known about this topic?
Exome and genome sequencing is increasingly used in prenatal diagnosis. Clinicians face numerous challenges in how to interpret genes and variants identified through prenatal sequencing.
What does this study add?
An international, multidisciplinary consortium allows for real‐time collaboration on ongoing cases, assessment of new technologies, and the opportunity to create a novel fetal sequencing repository.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>35661204</pmid><doi>10.1002/pd.6190</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-2265-0691</orcidid></addata></record> |
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source | Wiley Journals |
subjects | Fetuses |
title | The fetal sequencing consortium: The value of multidisciplinary dialog and collaboration |
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