Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1
Gespeichert in:
| Veröffentlicht in: | Human molecular genetics 2013-02, Vol.22 (4), p.696-703 |
|---|---|
| Hauptverfasser: | , , , , , , , , , , , , , , , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 703 |
|---|---|
| container_issue | 4 |
| container_start_page | 696 |
| container_title | Human molecular genetics |
| container_volume | 22 |
| creator | Slavotinek, A. M. Mehrotra, P. Nazarenko, I. Tang, P. L.-F. Lao, R. Cameron, D. Li, B. Chu, C. Chou, C. Marqueling, A. L. Yahyavi, M. Cordoro, K. Frieden, I. Glaser, T. Prescott, T. Morren, M.-A. Devriendt, K. Kwok, P.-y. Petkovich, M. Desnick, R. J. |
| description | |
| doi_str_mv | 10.1093/hmg/dds477 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1282049247</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1282049247</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2817-1e21d1b4f20f33135bd9a6fbc05dd2bde6457b3e3ac329e42d4d5991e3cb9d03</originalsourceid><addsrcrecordid>eNotkMtKw0AUQAdRsFY3fsEsRRo7r0w6SwlWCwVdFMHVMI8bHUmamJss8vdtqauzOZzFIeSesyfOjFz-NN_LGFEVxQWZcaVZJthKXpIZM1pl2jB9TW4QfxnjWsliRjbrNriaVi6kIyL0zQkTdrXD5BZ0mDqgm88FTUiDGxEi9RNtxsENqd0jTXtafn0IXfJbclW5GuHun3OyW7_syrds-_66KZ-3WRArXmQcBI_cq0qwSkoucx-N05UPLI9R-Aha5YWXIF2QwoASUcXcGA4yeBOZnJOHc7br278RcLBNwgB17fbQjmi5WAmmjFDFUX08q6FvEXuobNenxvWT5cyedtnjLnveJQ8CPVz4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1282049247</pqid></control><display><type>article</type><title>Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Slavotinek, A. M. ; Mehrotra, P. ; Nazarenko, I. ; Tang, P. L.-F. ; Lao, R. ; Cameron, D. ; Li, B. ; Chu, C. ; Chou, C. ; Marqueling, A. L. ; Yahyavi, M. ; Cordoro, K. ; Frieden, I. ; Glaser, T. ; Prescott, T. ; Morren, M.-A. ; Devriendt, K. ; Kwok, P.-y. ; Petkovich, M. ; Desnick, R. J.</creator><creatorcontrib>Slavotinek, A. M. ; Mehrotra, P. ; Nazarenko, I. ; Tang, P. L.-F. ; Lao, R. ; Cameron, D. ; Li, B. ; Chu, C. ; Chou, C. ; Marqueling, A. L. ; Yahyavi, M. ; Cordoro, K. ; Frieden, I. ; Glaser, T. ; Prescott, T. ; Morren, M.-A. ; Devriendt, K. ; Kwok, P.-y. ; Petkovich, M. ; Desnick, R. J.</creatorcontrib><identifier>ISSN: 0964-6906</identifier><identifier>EISSN: 1460-2083</identifier><identifier>DOI: 10.1093/hmg/dds477</identifier><language>eng</language><ispartof>Human molecular genetics, 2013-02, Vol.22 (4), p.696-703</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2817-1e21d1b4f20f33135bd9a6fbc05dd2bde6457b3e3ac329e42d4d5991e3cb9d03</citedby><cites>FETCH-LOGICAL-c2817-1e21d1b4f20f33135bd9a6fbc05dd2bde6457b3e3ac329e42d4d5991e3cb9d03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Slavotinek, A. M.</creatorcontrib><creatorcontrib>Mehrotra, P.</creatorcontrib><creatorcontrib>Nazarenko, I.</creatorcontrib><creatorcontrib>Tang, P. L.-F.</creatorcontrib><creatorcontrib>Lao, R.</creatorcontrib><creatorcontrib>Cameron, D.</creatorcontrib><creatorcontrib>Li, B.</creatorcontrib><creatorcontrib>Chu, C.</creatorcontrib><creatorcontrib>Chou, C.</creatorcontrib><creatorcontrib>Marqueling, A. L.</creatorcontrib><creatorcontrib>Yahyavi, M.</creatorcontrib><creatorcontrib>Cordoro, K.</creatorcontrib><creatorcontrib>Frieden, I.</creatorcontrib><creatorcontrib>Glaser, T.</creatorcontrib><creatorcontrib>Prescott, T.</creatorcontrib><creatorcontrib>Morren, M.-A.</creatorcontrib><creatorcontrib>Devriendt, K.</creatorcontrib><creatorcontrib>Kwok, P.-y.</creatorcontrib><creatorcontrib>Petkovich, M.</creatorcontrib><creatorcontrib>Desnick, R. J.</creatorcontrib><title>Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1</title><title>Human molecular genetics</title><issn>0964-6906</issn><issn>1460-2083</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNotkMtKw0AUQAdRsFY3fsEsRRo7r0w6SwlWCwVdFMHVMI8bHUmamJss8vdtqauzOZzFIeSesyfOjFz-NN_LGFEVxQWZcaVZJthKXpIZM1pl2jB9TW4QfxnjWsliRjbrNriaVi6kIyL0zQkTdrXD5BZ0mDqgm88FTUiDGxEi9RNtxsENqd0jTXtafn0IXfJbclW5GuHun3OyW7_syrds-_66KZ-3WRArXmQcBI_cq0qwSkoucx-N05UPLI9R-Aha5YWXIF2QwoASUcXcGA4yeBOZnJOHc7br278RcLBNwgB17fbQjmi5WAmmjFDFUX08q6FvEXuobNenxvWT5cyedtnjLnveJQ8CPVz4</recordid><startdate>20130215</startdate><enddate>20130215</enddate><creator>Slavotinek, A. M.</creator><creator>Mehrotra, P.</creator><creator>Nazarenko, I.</creator><creator>Tang, P. L.-F.</creator><creator>Lao, R.</creator><creator>Cameron, D.</creator><creator>Li, B.</creator><creator>Chu, C.</creator><creator>Chou, C.</creator><creator>Marqueling, A. L.</creator><creator>Yahyavi, M.</creator><creator>Cordoro, K.</creator><creator>Frieden, I.</creator><creator>Glaser, T.</creator><creator>Prescott, T.</creator><creator>Morren, M.-A.</creator><creator>Devriendt, K.</creator><creator>Kwok, P.-y.</creator><creator>Petkovich, M.</creator><creator>Desnick, R. J.</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20130215</creationdate><title>Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1</title><author>Slavotinek, A. M. ; Mehrotra, P. ; Nazarenko, I. ; Tang, P. L.-F. ; Lao, R. ; Cameron, D. ; Li, B. ; Chu, C. ; Chou, C. ; Marqueling, A. L. ; Yahyavi, M. ; Cordoro, K. ; Frieden, I. ; Glaser, T. ; Prescott, T. ; Morren, M.-A. ; Devriendt, K. ; Kwok, P.-y. ; Petkovich, M. ; Desnick, R. J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2817-1e21d1b4f20f33135bd9a6fbc05dd2bde6457b3e3ac329e42d4d5991e3cb9d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Slavotinek, A. M.</creatorcontrib><creatorcontrib>Mehrotra, P.</creatorcontrib><creatorcontrib>Nazarenko, I.</creatorcontrib><creatorcontrib>Tang, P. L.-F.</creatorcontrib><creatorcontrib>Lao, R.</creatorcontrib><creatorcontrib>Cameron, D.</creatorcontrib><creatorcontrib>Li, B.</creatorcontrib><creatorcontrib>Chu, C.</creatorcontrib><creatorcontrib>Chou, C.</creatorcontrib><creatorcontrib>Marqueling, A. L.</creatorcontrib><creatorcontrib>Yahyavi, M.</creatorcontrib><creatorcontrib>Cordoro, K.</creatorcontrib><creatorcontrib>Frieden, I.</creatorcontrib><creatorcontrib>Glaser, T.</creatorcontrib><creatorcontrib>Prescott, T.</creatorcontrib><creatorcontrib>Morren, M.-A.</creatorcontrib><creatorcontrib>Devriendt, K.</creatorcontrib><creatorcontrib>Kwok, P.-y.</creatorcontrib><creatorcontrib>Petkovich, M.</creatorcontrib><creatorcontrib>Desnick, R. J.</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Human molecular genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Slavotinek, A. M.</au><au>Mehrotra, P.</au><au>Nazarenko, I.</au><au>Tang, P. L.-F.</au><au>Lao, R.</au><au>Cameron, D.</au><au>Li, B.</au><au>Chu, C.</au><au>Chou, C.</au><au>Marqueling, A. L.</au><au>Yahyavi, M.</au><au>Cordoro, K.</au><au>Frieden, I.</au><au>Glaser, T.</au><au>Prescott, T.</au><au>Morren, M.-A.</au><au>Devriendt, K.</au><au>Kwok, P.-y.</au><au>Petkovich, M.</au><au>Desnick, R. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1</atitle><jtitle>Human molecular genetics</jtitle><date>2013-02-15</date><risdate>2013</risdate><volume>22</volume><issue>4</issue><spage>696</spage><epage>703</epage><pages>696-703</pages><issn>0964-6906</issn><eissn>1460-2083</eissn><doi>10.1093/hmg/dds477</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0964-6906 |
| ispartof | Human molecular genetics, 2013-02, Vol.22 (4), p.696-703 |
| issn | 0964-6906 1460-2083 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_1282049247 |
| source | Oxford University Press Journals All Titles (1996-Current); Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
| title | Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1 |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T19%3A57%3A04IST&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=Focal%20facial%20dermal%20dysplasia,%20type%20IV,%20is%20caused%20by%20mutations%20in%20CYP26C1&rft.jtitle=Human%20molecular%20genetics&rft.au=Slavotinek,%20A.%20M.&rft.date=2013-02-15&rft.volume=22&rft.issue=4&rft.spage=696&rft.epage=703&rft.pages=696-703&rft.issn=0964-6906&rft.eissn=1460-2083&rft_id=info:doi/10.1093/hmg/dds477&rft_dat=%3Cproquest_cross%3E1282049247%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=1282049247&rft_id=info:pmid/&rfr_iscdi=true |