An apparently nonsyndromic infant with the association of anorectal and cardiovascular anomalies and a 22q11 deletion

An apparently nonsyndromic infant with the association of anorectal and cardiovascular anomalies and a 22q11 deletion

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:American journal of medical genetics 2002-09, Vol.112 (1), p.114-115
Hauptverfasser: Rosti, Luca, Bini, Roberta M., Giamberti, Alessandro, Frigiola, Alessandro, Carminati, Mario
Format: Artikel
Sprache:eng
Schlagworte:
Anal Canal - abnormalities
Chromosome Deletion
Chromosomes, Human, Pair 22
Female
Heart Defects, Congenital - diagnosis
Humans
Infant, Newborn
Rectum - abnormalities
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 115
container_issue 1
container_start_page 114
container_title American journal of medical genetics
container_volume 112
creator Rosti, Luca
Bini, Roberta M.
Giamberti, Alessandro
Frigiola, Alessandro
Carminati, Mario
description
doi_str_mv 10.1002/ajmg.10620
format Article
fullrecord <record><control><sourceid>istex_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_ajmg_10620</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_646DN55V_1</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2910-3eaa553ebbdf8a4710066fd0a9bb4319202b71edc7456d09e001113dea4b8b833</originalsourceid><addsrcrecordid>eNp9kEtPwzAQhC0EoqVw4Qcgn5ECfiROcqwKFFApFx5HaxM71CVxip1S-u9J2gI3Trva_WakGYROKbmghLBLmFdv7SYY2UN9SlIRJIIl-6hPaJgEMUvTHjryfk4IbQ_sEPUoYzyNedhHy6HFsFiA07Yp19jW1q-tcnVlcmxsAbbBK9PMcDPTGLyvcwONqS2uCwy2djpvoGw3hXNwytSf4PNlCa57VlAa7TdPwIx9UIqVLnUnP0YHBZRen-zmAD3fXD-NboPJ4_huNJwEOUspCbgGiCKus0wVCYRxm1aIQhFIsyzkNGWEZTHVKo_DSCiS6i4h5UpDmCVZwvkAnW99c1d773QhF85U4NaSEtl1J7vu5Ka7Fj7bwotlVmn1h-7KagG6BVam1Ot_rOTw_mH8YxpsNcY3-utXA-5dipjHkXydjqUIxdU0il4k5d_xk4nU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>An apparently nonsyndromic infant with the association of anorectal and cardiovascular anomalies and a 22q11 deletion</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Rosti, Luca ; Bini, Roberta M. ; Giamberti, Alessandro ; Frigiola, Alessandro ; Carminati, Mario</creator><creatorcontrib>Rosti, Luca ; Bini, Roberta M. ; Giamberti, Alessandro ; Frigiola, Alessandro ; Carminati, Mario</creatorcontrib><identifier>ISSN: 0148-7299</identifier><identifier>EISSN: 1096-8628</identifier><identifier>DOI: 10.1002/ajmg.10620</identifier><identifier>PMID: 12239734</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Anal Canal - abnormalities ; Chromosome Deletion ; Chromosomes, Human, Pair 22 ; Female ; Heart Defects, Congenital - diagnosis ; Humans ; Infant, Newborn ; Rectum - abnormalities</subject><ispartof>American journal of medical genetics, 2002-09, Vol.112 (1), p.114-115</ispartof><rights>Copyright © 2002 Wiley‐Liss, Inc.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2910-3eaa553ebbdf8a4710066fd0a9bb4319202b71edc7456d09e001113dea4b8b833</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12239734$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rosti, Luca</creatorcontrib><creatorcontrib>Bini, Roberta M.</creatorcontrib><creatorcontrib>Giamberti, Alessandro</creatorcontrib><creatorcontrib>Frigiola, Alessandro</creatorcontrib><creatorcontrib>Carminati, Mario</creatorcontrib><title>An apparently nonsyndromic infant with the association of anorectal and cardiovascular anomalies and a 22q11 deletion</title><title>American journal of medical genetics</title><addtitle>Am. J. Med. Genet</addtitle><subject>Anal Canal - abnormalities</subject><subject>Chromosome Deletion</subject><subject>Chromosomes, Human, Pair 22</subject><subject>Female</subject><subject>Heart Defects, Congenital - diagnosis</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Rectum - abnormalities</subject><issn>0148-7299</issn><issn>1096-8628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtPwzAQhC0EoqVw4Qcgn5ECfiROcqwKFFApFx5HaxM71CVxip1S-u9J2gI3Trva_WakGYROKbmghLBLmFdv7SYY2UN9SlIRJIIl-6hPaJgEMUvTHjryfk4IbQ_sEPUoYzyNedhHy6HFsFiA07Yp19jW1q-tcnVlcmxsAbbBK9PMcDPTGLyvcwONqS2uCwy2djpvoGw3hXNwytSf4PNlCa57VlAa7TdPwIx9UIqVLnUnP0YHBZRen-zmAD3fXD-NboPJ4_huNJwEOUspCbgGiCKus0wVCYRxm1aIQhFIsyzkNGWEZTHVKo_DSCiS6i4h5UpDmCVZwvkAnW99c1d773QhF85U4NaSEtl1J7vu5Ka7Fj7bwotlVmn1h-7KagG6BVam1Ot_rOTw_mH8YxpsNcY3-utXA-5dipjHkXydjqUIxdU0il4k5d_xk4nU</recordid><startdate>20020915</startdate><enddate>20020915</enddate><creator>Rosti, Luca</creator><creator>Bini, Roberta M.</creator><creator>Giamberti, Alessandro</creator><creator>Frigiola, Alessandro</creator><creator>Carminati, Mario</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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></search><sort><creationdate>20020915</creationdate><title>An apparently nonsyndromic infant with the association of anorectal and cardiovascular anomalies and a 22q11 deletion</title><author>Rosti, Luca ; Bini, Roberta M. ; Giamberti, Alessandro ; Frigiola, Alessandro ; Carminati, Mario</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2910-3eaa553ebbdf8a4710066fd0a9bb4319202b71edc7456d09e001113dea4b8b833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Anal Canal - abnormalities</topic><topic>Chromosome Deletion</topic><topic>Chromosomes, Human, Pair 22</topic><topic>Female</topic><topic>Heart Defects, Congenital - diagnosis</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Rectum - abnormalities</topic><toplevel>online_resources</toplevel><creatorcontrib>Rosti, Luca</creatorcontrib><creatorcontrib>Bini, Roberta M.</creatorcontrib><creatorcontrib>Giamberti, Alessandro</creatorcontrib><creatorcontrib>Frigiola, Alessandro</creatorcontrib><creatorcontrib>Carminati, Mario</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>American journal of medical genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rosti, Luca</au><au>Bini, Roberta M.</au><au>Giamberti, Alessandro</au><au>Frigiola, Alessandro</au><au>Carminati, Mario</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An apparently nonsyndromic infant with the association of anorectal and cardiovascular anomalies and a 22q11 deletion</atitle><jtitle>American journal of medical genetics</jtitle><addtitle>Am. J. Med. Genet</addtitle><date>2002-09-15</date><risdate>2002</risdate><volume>112</volume><issue>1</issue><spage>114</spage><epage>115</epage><pages>114-115</pages><issn>0148-7299</issn><eissn>1096-8628</eissn><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>12239734</pmid><doi>10.1002/ajmg.10620</doi><tpages>2</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0148-7299
ispartof American journal of medical genetics, 2002-09, Vol.112 (1), p.114-115
issn 0148-7299
1096-8628
language eng
recordid cdi_crossref_primary_10_1002_ajmg_10620
source MEDLINE; Alma/SFX Local Collection
subjects Anal Canal - abnormalities
Chromosome Deletion
Chromosomes, Human, Pair 22
Female
Heart Defects, Congenital - diagnosis
Humans
Infant, Newborn
Rectum - abnormalities
title An apparently nonsyndromic infant with the association of anorectal and cardiovascular anomalies and a 22q11 deletion
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T13%3A01%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=An%20apparently%20nonsyndromic%20infant%20with%20the%20association%20of%20anorectal%20and%20cardiovascular%20anomalies%20and%20a%2022q11%20deletion&rft.jtitle=American%20journal%20of%20medical%20genetics&rft.au=Rosti,%20Luca&rft.date=2002-09-15&rft.volume=112&rft.issue=1&rft.spage=114&rft.epage=115&rft.pages=114-115&rft.issn=0148-7299&rft.eissn=1096-8628&rft_id=info:doi/10.1002/ajmg.10620&rft_dat=%3Cistex_cross%3Eark_67375_WNG_646DN55V_1%3C/istex_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/12239734&rfr_iscdi=true