Diaphragmatic hernia in 18p- syndrome
Gespeichert in:
| Veröffentlicht in: | American journal of medical genetics 2004-02, Vol.125A (1), p.97-99 |
|---|---|
| Hauptverfasser: | , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 99 |
|---|---|
| container_issue | 1 |
| container_start_page | 97 |
| container_title | American journal of medical genetics |
| container_volume | 125A |
| creator | Strenge, Sibylle Froster, Ursula G. |
| description | |
| doi_str_mv | 10.1002/ajmg.a.20459 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_80145127</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>80145127</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4309-cd2db6c314bd1e44b08a6f611d6f291103a0a182abb9270fbf0bafa9226c108f3</originalsourceid><addsrcrecordid>eNqF0DtPwzAQB3ALgXhvzKgLTKScn0lG1EIB8Rp4bdbFsVtDkha7FfTb09ICGwynu-F3d9KfkD0KbQrAjvGl7rexzUDIfIVsUilZIjLOV39mJjfIVowvABxkqtbJBhWplLPaJAddj6NBwH6NY29aAxsajy3ftGg2Slpx2pRhWNsdsuawinZ32bfJw9npfec8ubrtXXROrhIjOOSJKVlZKMOpKEpqhSggQ-UUpaVyLKcUOALSjGFR5CwFVzgo0GHOmDIUMse3yeHi7igM3yY2jnXto7FVhY0dTqLOgApJWfovZJBlIHM-g0cLaMIwxmCdHgVfY5hqCnqen57np1F_5Tfj-8u7k6K25S9eBjYDB0uA0WDlAjbGx18nhVQinzu-cO--stM_n-qTy-ve9_tkseXj2H78bGF41SrlqdRPNz3dfbxLpXpONfBPkciVnQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20880593</pqid></control><display><type>article</type><title>Diaphragmatic hernia in 18p- syndrome</title><source>MEDLINE</source><source>Wiley Journals</source><creator>Strenge, Sibylle ; Froster, Ursula G.</creator><creatorcontrib>Strenge, Sibylle ; Froster, Ursula G.</creatorcontrib><identifier>ISSN: 1552-4825</identifier><identifier>ISSN: 0148-7299</identifier><identifier>EISSN: 1552-4833</identifier><identifier>EISSN: 1096-8628</identifier><identifier>DOI: 10.1002/ajmg.a.20459</identifier><identifier>PMID: 14755475</identifier><identifier>CODEN: AJMGDA</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Abnormalities, Multiple - genetics ; Abnormalities, Multiple - pathology ; Biological and medical sciences ; Chromosome Deletion ; Chromosomes, Human, Pair 18 - genetics ; Female ; General aspects. Genetic counseling ; Hernia, Diaphragmatic - pathology ; Humans ; Infant ; Karyotyping ; Medical genetics ; Medical sciences ; Syndrome</subject><ispartof>American journal of medical genetics, 2004-02, Vol.125A (1), p.97-99</ispartof><rights>Copyright © 2003 Wiley‐Liss, Inc.</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4309-cd2db6c314bd1e44b08a6f611d6f291103a0a182abb9270fbf0bafa9226c108f3</citedby><cites>FETCH-LOGICAL-c4309-cd2db6c314bd1e44b08a6f611d6f291103a0a182abb9270fbf0bafa9226c108f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fajmg.a.20459$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fajmg.a.20459$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15456495$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14755475$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Strenge, Sibylle</creatorcontrib><creatorcontrib>Froster, Ursula G.</creatorcontrib><title>Diaphragmatic hernia in 18p- syndrome</title><title>American journal of medical genetics</title><addtitle>Am. J. Med. Genet</addtitle><subject>Abnormalities, Multiple - genetics</subject><subject>Abnormalities, Multiple - pathology</subject><subject>Biological and medical sciences</subject><subject>Chromosome Deletion</subject><subject>Chromosomes, Human, Pair 18 - genetics</subject><subject>Female</subject><subject>General aspects. Genetic counseling</subject><subject>Hernia, Diaphragmatic - pathology</subject><subject>Humans</subject><subject>Infant</subject><subject>Karyotyping</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Syndrome</subject><issn>1552-4825</issn><issn>0148-7299</issn><issn>1552-4833</issn><issn>1096-8628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0DtPwzAQB3ALgXhvzKgLTKScn0lG1EIB8Rp4bdbFsVtDkha7FfTb09ICGwynu-F3d9KfkD0KbQrAjvGl7rexzUDIfIVsUilZIjLOV39mJjfIVowvABxkqtbJBhWplLPaJAddj6NBwH6NY29aAxsajy3ftGg2Slpx2pRhWNsdsuawinZ32bfJw9npfec8ubrtXXROrhIjOOSJKVlZKMOpKEpqhSggQ-UUpaVyLKcUOALSjGFR5CwFVzgo0GHOmDIUMse3yeHi7igM3yY2jnXto7FVhY0dTqLOgApJWfovZJBlIHM-g0cLaMIwxmCdHgVfY5hqCnqen57np1F_5Tfj-8u7k6K25S9eBjYDB0uA0WDlAjbGx18nhVQinzu-cO--stM_n-qTy-ve9_tkseXj2H78bGF41SrlqdRPNz3dfbxLpXpONfBPkciVnQ</recordid><startdate>20040215</startdate><enddate>20040215</enddate><creator>Strenge, Sibylle</creator><creator>Froster, Ursula G.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20040215</creationdate><title>Diaphragmatic hernia in 18p- syndrome</title><author>Strenge, Sibylle ; Froster, Ursula G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4309-cd2db6c314bd1e44b08a6f611d6f291103a0a182abb9270fbf0bafa9226c108f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Abnormalities, Multiple - genetics</topic><topic>Abnormalities, Multiple - pathology</topic><topic>Biological and medical sciences</topic><topic>Chromosome Deletion</topic><topic>Chromosomes, Human, Pair 18 - genetics</topic><topic>Female</topic><topic>General aspects. Genetic counseling</topic><topic>Hernia, Diaphragmatic - pathology</topic><topic>Humans</topic><topic>Infant</topic><topic>Karyotyping</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Syndrome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Strenge, Sibylle</creatorcontrib><creatorcontrib>Froster, Ursula G.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of medical genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Strenge, Sibylle</au><au>Froster, Ursula G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diaphragmatic hernia in 18p- syndrome</atitle><jtitle>American journal of medical genetics</jtitle><addtitle>Am. J. Med. Genet</addtitle><date>2004-02-15</date><risdate>2004</risdate><volume>125A</volume><issue>1</issue><spage>97</spage><epage>99</epage><pages>97-99</pages><issn>1552-4825</issn><issn>0148-7299</issn><eissn>1552-4833</eissn><eissn>1096-8628</eissn><coden>AJMGDA</coden><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>14755475</pmid><doi>10.1002/ajmg.a.20459</doi><tpages>3</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1552-4825 |
| ispartof | American journal of medical genetics, 2004-02, Vol.125A (1), p.97-99 |
| issn | 1552-4825 0148-7299 1552-4833 1096-8628 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_80145127 |
| source | MEDLINE; Wiley Journals |
| subjects | Abnormalities, Multiple - genetics Abnormalities, Multiple - pathology Biological and medical sciences Chromosome Deletion Chromosomes, Human, Pair 18 - genetics Female General aspects. Genetic counseling Hernia, Diaphragmatic - pathology Humans Infant Karyotyping Medical genetics Medical sciences Syndrome |
| title | Diaphragmatic hernia in 18p- syndrome |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T11%3A08%3A27IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Diaphragmatic%20hernia%20in%2018p-%20syndrome&rft.jtitle=American%20journal%20of%20medical%20genetics&rft.au=Strenge,%20Sibylle&rft.date=2004-02-15&rft.volume=125A&rft.issue=1&rft.spage=97&rft.epage=99&rft.pages=97-99&rft.issn=1552-4825&rft.eissn=1552-4833&rft.coden=AJMGDA&rft_id=info:doi/10.1002/ajmg.a.20459&rft_dat=%3Cproquest_cross%3E80145127%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=20880593&rft_id=info:pmid/14755475&rfr_iscdi=true |