Loading…
Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome
Saved in:
| Published in: | American journal of human genetics 2000, Vol.66 (1), p.312-319 |
|---|---|
| Main Authors: | , , , , , , , , , |
| Format: | Article |
| Language: | English |
| Subjects: | |
| Citations: | Items that this one cites Items that cite this one |
| Online Access: | Get full text |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| cited_by | cdi_FETCH-LOGICAL-c403t-a6b15822aae636a4530839b832d64aca9e2c08098bcc60dde86b71288650547c3 |
|---|---|
| cites | cdi_FETCH-LOGICAL-c403t-a6b15822aae636a4530839b832d64aca9e2c08098bcc60dde86b71288650547c3 |
| container_end_page | 319 |
| container_issue | 1 |
| container_start_page | 312 |
| container_title | American journal of human genetics |
| container_volume | 66 |
| creator | Belloni, E. Martucciello, G. Verderio, D. Ponti, E. Seri, M. Jasonni, V. Torre, M. Ferrari, M. Tsui, L.-C. Scherer, S.W. |
| description | |
| doi_str_mv | 10.1086/302723 |
| format | article |
| fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1288336</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0002929707622563</els_id><sourcerecordid>70894212</sourcerecordid><originalsourceid>FETCH-LOGICAL-c403t-a6b15822aae636a4530839b832d64aca9e2c08098bcc60dde86b71288650547c3</originalsourceid><addsrcrecordid>eNpdkF1LwzAUhoMoOqf-BOmVd9WTpE1TEEGHusHACxW8C2l65iJtMpNu6L-3Y8Ovq3PxPjzn5SXkhMI5BSkuOLCC8R0yoDkvUiEg3yUDAGBpycrigBzG-AZAqQS-Tw4oCE6pgAG5nLiVb1bYousSP0u6OSbj6ctNmYx9i77yH8k9OkysS0bLEHSwziePn64OfXxE9ma6iXi8vUPyfHf7NBqn04f7yeh6mpoMeJdqUdFcMqY1Ci50lnOQvKwkZ7XItNElMgMSSlkZI6CuUYqqoExKkUOeFYYPydXGu1hWLdam7xp0oxbBtjp8Kq-t-ps4O1evfqXWEs5FLzjbCoJ_X2LsVGujwabRDv0yqgJkmTHKfkATfIwBZ99PKKj10GozdA-e_q70C9ss2wOwAbAfZmUxqGgsOoO1DWg6VXv73_kFmLqGxQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70894212</pqid></control><display><type>article</type><title>Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome</title><source>BACON - Elsevier - GLOBAL_SCIENCEDIRECT-OPENACCESS</source><source>PubMed Central Free</source><creator>Belloni, E. ; Martucciello, G. ; Verderio, D. ; Ponti, E. ; Seri, M. ; Jasonni, V. ; Torre, M. ; Ferrari, M. ; Tsui, L.-C. ; Scherer, S.W.</creator><creatorcontrib>Belloni, E. ; Martucciello, G. ; Verderio, D. ; Ponti, E. ; Seri, M. ; Jasonni, V. ; Torre, M. ; Ferrari, M. ; Tsui, L.-C. ; Scherer, S.W.</creatorcontrib><identifier>ISSN: 0002-9297</identifier><identifier>EISSN: 1537-6605</identifier><identifier>DOI: 10.1086/302723</identifier><identifier>PMID: 10631160</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Abnormalities, Multiple - diagnostic imaging ; Abnormalities, Multiple - genetics ; Anal Canal - abnormalities ; CGC length variation ; Currarino syndrome ; DNA Mutational Analysis ; HLXB9 ; Homeodomain Proteins - genetics ; Humans ; Letters to the Editor ; Magnetic Resonance Imaging ; Meningocele - genetics ; Radiography ; Rectum - abnormalities ; Sacrum - abnormalities ; Syndrome ; Transcription Factors - genetics</subject><ispartof>American journal of human genetics, 2000, Vol.66 (1), p.312-319</ispartof><rights>2000 The American Society of Human Genetics</rights><rights>2000 by The American Society of Human Genetics. All rights reserved. 2000</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c403t-a6b15822aae636a4530839b832d64aca9e2c08098bcc60dde86b71288650547c3</citedby><cites>FETCH-LOGICAL-c403t-a6b15822aae636a4530839b832d64aca9e2c08098bcc60dde86b71288650547c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1288336/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1288336/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,27923,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10631160$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Belloni, E.</creatorcontrib><creatorcontrib>Martucciello, G.</creatorcontrib><creatorcontrib>Verderio, D.</creatorcontrib><creatorcontrib>Ponti, E.</creatorcontrib><creatorcontrib>Seri, M.</creatorcontrib><creatorcontrib>Jasonni, V.</creatorcontrib><creatorcontrib>Torre, M.</creatorcontrib><creatorcontrib>Ferrari, M.</creatorcontrib><creatorcontrib>Tsui, L.-C.</creatorcontrib><creatorcontrib>Scherer, S.W.</creatorcontrib><title>Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome</title><title>American journal of human genetics</title><addtitle>Am J Hum Genet</addtitle><subject>Abnormalities, Multiple - diagnostic imaging</subject><subject>Abnormalities, Multiple - genetics</subject><subject>Anal Canal - abnormalities</subject><subject>CGC length variation</subject><subject>Currarino syndrome</subject><subject>DNA Mutational Analysis</subject><subject>HLXB9</subject><subject>Homeodomain Proteins - genetics</subject><subject>Humans</subject><subject>Letters to the Editor</subject><subject>Magnetic Resonance Imaging</subject><subject>Meningocele - genetics</subject><subject>Radiography</subject><subject>Rectum - abnormalities</subject><subject>Sacrum - abnormalities</subject><subject>Syndrome</subject><subject>Transcription Factors - genetics</subject><issn>0002-9297</issn><issn>1537-6605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNpdkF1LwzAUhoMoOqf-BOmVd9WTpE1TEEGHusHACxW8C2l65iJtMpNu6L-3Y8Ovq3PxPjzn5SXkhMI5BSkuOLCC8R0yoDkvUiEg3yUDAGBpycrigBzG-AZAqQS-Tw4oCE6pgAG5nLiVb1bYousSP0u6OSbj6ctNmYx9i77yH8k9OkysS0bLEHSwziePn64OfXxE9ma6iXi8vUPyfHf7NBqn04f7yeh6mpoMeJdqUdFcMqY1Ci50lnOQvKwkZ7XItNElMgMSSlkZI6CuUYqqoExKkUOeFYYPydXGu1hWLdam7xp0oxbBtjp8Kq-t-ps4O1evfqXWEs5FLzjbCoJ_X2LsVGujwabRDv0yqgJkmTHKfkATfIwBZ99PKKj10GozdA-e_q70C9ss2wOwAbAfZmUxqGgsOoO1DWg6VXv73_kFmLqGxQ</recordid><startdate>2000</startdate><enddate>2000</enddate><creator>Belloni, E.</creator><creator>Martucciello, G.</creator><creator>Verderio, D.</creator><creator>Ponti, E.</creator><creator>Seri, M.</creator><creator>Jasonni, V.</creator><creator>Torre, M.</creator><creator>Ferrari, M.</creator><creator>Tsui, L.-C.</creator><creator>Scherer, S.W.</creator><general>Elsevier Inc</general><general>The American Society of Human Genetics</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>2000</creationdate><title>Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome</title><author>Belloni, E. ; Martucciello, G. ; Verderio, D. ; Ponti, E. ; Seri, M. ; Jasonni, V. ; Torre, M. ; Ferrari, M. ; Tsui, L.-C. ; Scherer, S.W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c403t-a6b15822aae636a4530839b832d64aca9e2c08098bcc60dde86b71288650547c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Abnormalities, Multiple - diagnostic imaging</topic><topic>Abnormalities, Multiple - genetics</topic><topic>Anal Canal - abnormalities</topic><topic>CGC length variation</topic><topic>Currarino syndrome</topic><topic>DNA Mutational Analysis</topic><topic>HLXB9</topic><topic>Homeodomain Proteins - genetics</topic><topic>Humans</topic><topic>Letters to the Editor</topic><topic>Magnetic Resonance Imaging</topic><topic>Meningocele - genetics</topic><topic>Radiography</topic><topic>Rectum - abnormalities</topic><topic>Sacrum - abnormalities</topic><topic>Syndrome</topic><topic>Transcription Factors - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Belloni, E.</creatorcontrib><creatorcontrib>Martucciello, G.</creatorcontrib><creatorcontrib>Verderio, D.</creatorcontrib><creatorcontrib>Ponti, E.</creatorcontrib><creatorcontrib>Seri, M.</creatorcontrib><creatorcontrib>Jasonni, V.</creatorcontrib><creatorcontrib>Torre, M.</creatorcontrib><creatorcontrib>Ferrari, M.</creatorcontrib><creatorcontrib>Tsui, L.-C.</creatorcontrib><creatorcontrib>Scherer, S.W.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of human genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Belloni, E.</au><au>Martucciello, G.</au><au>Verderio, D.</au><au>Ponti, E.</au><au>Seri, M.</au><au>Jasonni, V.</au><au>Torre, M.</au><au>Ferrari, M.</au><au>Tsui, L.-C.</au><au>Scherer, S.W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome</atitle><jtitle>American journal of human genetics</jtitle><addtitle>Am J Hum Genet</addtitle><date>2000</date><risdate>2000</risdate><volume>66</volume><issue>1</issue><spage>312</spage><epage>319</epage><pages>312-319</pages><issn>0002-9297</issn><eissn>1537-6605</eissn><cop>United States</cop><pub>Elsevier Inc</pub><pmid>10631160</pmid><doi>10.1086/302723</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0002-9297 |
| ispartof | American journal of human genetics, 2000, Vol.66 (1), p.312-319 |
| issn | 0002-9297 1537-6605 |
| language | eng |
| recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1288336 |
| source | BACON - Elsevier - GLOBAL_SCIENCEDIRECT-OPENACCESS; PubMed Central Free |
| subjects | Abnormalities, Multiple - diagnostic imaging Abnormalities, Multiple - genetics Anal Canal - abnormalities CGC length variation Currarino syndrome DNA Mutational Analysis HLXB9 Homeodomain Proteins - genetics Humans Letters to the Editor Magnetic Resonance Imaging Meningocele - genetics Radiography Rectum - abnormalities Sacrum - abnormalities Syndrome Transcription Factors - genetics |
| title | Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome |
| url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T19%3A57%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Involvement%20of%20the%20HLXB9%20Homeobox%20Gene%20in%20Currarino%20Syndrome&rft.jtitle=American%20journal%20of%20human%20genetics&rft.au=Belloni,%20E.&rft.date=2000&rft.volume=66&rft.issue=1&rft.spage=312&rft.epage=319&rft.pages=312-319&rft.issn=0002-9297&rft.eissn=1537-6605&rft_id=info:doi/10.1086/302723&rft_dat=%3Cproquest_pubme%3E70894212%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c403t-a6b15822aae636a4530839b832d64aca9e2c08098bcc60dde86b71288650547c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=70894212&rft_id=info:pmid/10631160&rfr_iscdi=true |