Brief Report: A Case of Autism Associated with del(2)(q32.1q32.2) or (q32.2q32.3)
This paper reports a clinical case of autism with a deletion on chromosome 2 in a young male with high functioning autism. The deletion seems to correspond with regions emerging from linkage studies. The paper proposes this chromosomal region as a possible candidate region in the search for autism g...
Gespeichert in:
Veröffentlicht in: | Journal of autism and developmental disorders 2003-02, Vol.33 (1), p.105-108 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 108 |
---|---|
container_issue | 1 |
container_start_page | 105 |
container_title | Journal of autism and developmental disorders |
container_volume | 33 |
creator | Gallagher, Louise Becker, Kristin Kearney, Geraldine Dunlop, Adam Stallings, Ray Green, Andrew Fitzgerald, Michael Gill, Michael |
description | This paper reports a clinical case of autism with a deletion on chromosome 2 in a young male with high functioning autism. The deletion seems to correspond with regions emerging from linkage studies. The paper proposes this chromosomal region as a possible candidate region in the search for autism genes. (Contains references.) (Author/DB) |
doi_str_mv | 10.1023/A:1022242807513 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_73200932</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><ericid>EJ664542</ericid><sourcerecordid>977900931</sourcerecordid><originalsourceid>FETCH-LOGICAL-c301t-d2588e5b0106b0cd5f9e8a7228f8f4c26091e22a3f034c4125d6f479bec2925f3</originalsourceid><addsrcrecordid>eNpdkM1Lw0AQxRdRbK2evYgsHqQ9pO7O7Cab3mKpXxRE0XNINruYkjbtboL435va6sHLewzzY5j3CDnnbMwZ4E0y6QxAgGKR5HhA-lxGGKBAOCR9xkMIEGTUIyfeLxhjsQI4Jj0OEVNShX3ycutKY-mrWdeumdCETjNvaG1p0jalX9LE-1qXWWMK-lk2H7Qw1RBGww3CmG8FRrR29GeGreDolBzZrPLmbO8D8n43e5s-BPPn-8dpMg80Mt4EBUiljMwZZ2HOdCFtbFQWASirrNAQspgbgAwtQ6EFB1mEVkRxbjTEIC0OyPXu7trVm9b4Jl2WXpuqylambn0aIXR5ETrw6h-4qFu36n5LgUmIY-wqG5DLPdTmS1Oka1cuM_eV_jbVARc7wLhS_61nT2EopAD8BupabOc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>205299357</pqid></control><display><type>article</type><title>Brief Report: A Case of Autism Associated with del(2)(q32.1q32.2) or (q32.2q32.3)</title><source>Applied Social Sciences Index & Abstracts (ASSIA)</source><source>MEDLINE</source><source>Education Source</source><source>SpringerLink Journals - AutoHoldings</source><creator>Gallagher, Louise ; Becker, Kristin ; Kearney, Geraldine ; Dunlop, Adam ; Stallings, Ray ; Green, Andrew ; Fitzgerald, Michael ; Gill, Michael</creator><creatorcontrib>Gallagher, Louise ; Becker, Kristin ; Kearney, Geraldine ; Dunlop, Adam ; Stallings, Ray ; Green, Andrew ; Fitzgerald, Michael ; Gill, Michael</creatorcontrib><description>This paper reports a clinical case of autism with a deletion on chromosome 2 in a young male with high functioning autism. The deletion seems to correspond with regions emerging from linkage studies. The paper proposes this chromosomal region as a possible candidate region in the search for autism genes. (Contains references.) (Author/DB)</description><identifier>ISSN: 0162-3257</identifier><identifier>EISSN: 1573-3432</identifier><identifier>DOI: 10.1023/A:1022242807513</identifier><identifier>PMID: 12708586</identifier><identifier>CODEN: JADDDQ</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Academic Achievement ; Adolescent ; Algorithms ; Autism ; Autistic Disorder - genetics ; Case Studies ; Chromosome Abnormalities ; Chromosomes, Human, Pair 2 - genetics ; Comprehension ; Cytogenetics - methods ; Departments ; Developmental Delays ; Elementary Education ; Etiology ; Evidence ; Gene Deletion ; Genetics ; Humans ; Imagination ; Interpersonal Relationship ; Karyotyping ; Learning Disabilities ; Male ; Males ; Mathematics ; Medical Evaluation ; Nonverbal Communication ; Performance Based Assessment ; Physical Development ; Physical Examinations ; Point Mutation - genetics ; Pregnancy ; Psychological Evaluation ; Research Needs ; Research Tools ; Special Needs Students ; Toilet Training</subject><ispartof>Journal of autism and developmental disorders, 2003-02, Vol.33 (1), p.105-108</ispartof><rights>Plenum Publishing Corporation 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c301t-d2588e5b0106b0cd5f9e8a7228f8f4c26091e22a3f034c4125d6f479bec2925f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,12825,27901,27902,30976</link.rule.ids><backlink>$$Uhttp://eric.ed.gov/ERICWebPortal/detail?accno=EJ664542$$DView record in ERIC$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12708586$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gallagher, Louise</creatorcontrib><creatorcontrib>Becker, Kristin</creatorcontrib><creatorcontrib>Kearney, Geraldine</creatorcontrib><creatorcontrib>Dunlop, Adam</creatorcontrib><creatorcontrib>Stallings, Ray</creatorcontrib><creatorcontrib>Green, Andrew</creatorcontrib><creatorcontrib>Fitzgerald, Michael</creatorcontrib><creatorcontrib>Gill, Michael</creatorcontrib><title>Brief Report: A Case of Autism Associated with del(2)(q32.1q32.2) or (q32.2q32.3)</title><title>Journal of autism and developmental disorders</title><addtitle>J Autism Dev Disord</addtitle><description>This paper reports a clinical case of autism with a deletion on chromosome 2 in a young male with high functioning autism. The deletion seems to correspond with regions emerging from linkage studies. The paper proposes this chromosomal region as a possible candidate region in the search for autism genes. (Contains references.) (Author/DB)</description><subject>Academic Achievement</subject><subject>Adolescent</subject><subject>Algorithms</subject><subject>Autism</subject><subject>Autistic Disorder - genetics</subject><subject>Case Studies</subject><subject>Chromosome Abnormalities</subject><subject>Chromosomes, Human, Pair 2 - genetics</subject><subject>Comprehension</subject><subject>Cytogenetics - methods</subject><subject>Departments</subject><subject>Developmental Delays</subject><subject>Elementary Education</subject><subject>Etiology</subject><subject>Evidence</subject><subject>Gene Deletion</subject><subject>Genetics</subject><subject>Humans</subject><subject>Imagination</subject><subject>Interpersonal Relationship</subject><subject>Karyotyping</subject><subject>Learning Disabilities</subject><subject>Male</subject><subject>Males</subject><subject>Mathematics</subject><subject>Medical Evaluation</subject><subject>Nonverbal Communication</subject><subject>Performance Based Assessment</subject><subject>Physical Development</subject><subject>Physical Examinations</subject><subject>Point Mutation - genetics</subject><subject>Pregnancy</subject><subject>Psychological Evaluation</subject><subject>Research Needs</subject><subject>Research Tools</subject><subject>Special Needs Students</subject><subject>Toilet Training</subject><issn>0162-3257</issn><issn>1573-3432</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkM1Lw0AQxRdRbK2evYgsHqQ9pO7O7Cab3mKpXxRE0XNINruYkjbtboL435va6sHLewzzY5j3CDnnbMwZ4E0y6QxAgGKR5HhA-lxGGKBAOCR9xkMIEGTUIyfeLxhjsQI4Jj0OEVNShX3ycutKY-mrWdeumdCETjNvaG1p0jalX9LE-1qXWWMK-lk2H7Qw1RBGww3CmG8FRrR29GeGreDolBzZrPLmbO8D8n43e5s-BPPn-8dpMg80Mt4EBUiljMwZZ2HOdCFtbFQWASirrNAQspgbgAwtQ6EFB1mEVkRxbjTEIC0OyPXu7trVm9b4Jl2WXpuqylambn0aIXR5ETrw6h-4qFu36n5LgUmIY-wqG5DLPdTmS1Oka1cuM_eV_jbVARc7wLhS_61nT2EopAD8BupabOc</recordid><startdate>20030201</startdate><enddate>20030201</enddate><creator>Gallagher, Louise</creator><creator>Becker, Kristin</creator><creator>Kearney, Geraldine</creator><creator>Dunlop, Adam</creator><creator>Stallings, Ray</creator><creator>Green, Andrew</creator><creator>Fitzgerald, Michael</creator><creator>Gill, Michael</creator><general>Springer Nature B.V</general><scope>7SW</scope><scope>BJH</scope><scope>BNH</scope><scope>BNI</scope><scope>BNJ</scope><scope>BNO</scope><scope>ERI</scope><scope>PET</scope><scope>REK</scope><scope>WWN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>0-V</scope><scope>3V.</scope><scope>7QJ</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88B</scope><scope>88E</scope><scope>88G</scope><scope>88J</scope><scope>8A4</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>CJNVE</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HEHIP</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0P</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2R</scope><scope>M2S</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEDU</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20030201</creationdate><title>Brief Report: A Case of Autism Associated with del(2)(q32.1q32.2) or (q32.2q32.3)</title><author>Gallagher, Louise ; Becker, Kristin ; Kearney, Geraldine ; Dunlop, Adam ; Stallings, Ray ; Green, Andrew ; Fitzgerald, Michael ; Gill, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c301t-d2588e5b0106b0cd5f9e8a7228f8f4c26091e22a3f034c4125d6f479bec2925f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Academic Achievement</topic><topic>Adolescent</topic><topic>Algorithms</topic><topic>Autism</topic><topic>Autistic Disorder - genetics</topic><topic>Case Studies</topic><topic>Chromosome Abnormalities</topic><topic>Chromosomes, Human, Pair 2 - genetics</topic><topic>Comprehension</topic><topic>Cytogenetics - methods</topic><topic>Departments</topic><topic>Developmental Delays</topic><topic>Elementary Education</topic><topic>Etiology</topic><topic>Evidence</topic><topic>Gene Deletion</topic><topic>Genetics</topic><topic>Humans</topic><topic>Imagination</topic><topic>Interpersonal Relationship</topic><topic>Karyotyping</topic><topic>Learning Disabilities</topic><topic>Male</topic><topic>Males</topic><topic>Mathematics</topic><topic>Medical Evaluation</topic><topic>Nonverbal Communication</topic><topic>Performance Based Assessment</topic><topic>Physical Development</topic><topic>Physical Examinations</topic><topic>Point Mutation - genetics</topic><topic>Pregnancy</topic><topic>Psychological Evaluation</topic><topic>Research Needs</topic><topic>Research Tools</topic><topic>Special Needs Students</topic><topic>Toilet Training</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gallagher, Louise</creatorcontrib><creatorcontrib>Becker, Kristin</creatorcontrib><creatorcontrib>Kearney, Geraldine</creatorcontrib><creatorcontrib>Dunlop, Adam</creatorcontrib><creatorcontrib>Stallings, Ray</creatorcontrib><creatorcontrib>Green, Andrew</creatorcontrib><creatorcontrib>Fitzgerald, Michael</creatorcontrib><creatorcontrib>Gill, Michael</creatorcontrib><collection>ERIC</collection><collection>ERIC (Ovid)</collection><collection>ERIC</collection><collection>ERIC</collection><collection>ERIC (Legacy Platform)</collection><collection>ERIC( SilverPlatter )</collection><collection>ERIC</collection><collection>ERIC PlusText (Legacy Platform)</collection><collection>Education Resources Information Center (ERIC)</collection><collection>ERIC</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Social Sciences Premium Collection</collection><collection>ProQuest Central (Corporate)</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Education Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Social Science Database (Alumni Edition)</collection><collection>Education Periodicals</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Social Science Premium Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Education Collection</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Sociology Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Education Database</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Research Library</collection><collection>Social Science Database</collection><collection>Sociology Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Education</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of autism and developmental disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gallagher, Louise</au><au>Becker, Kristin</au><au>Kearney, Geraldine</au><au>Dunlop, Adam</au><au>Stallings, Ray</au><au>Green, Andrew</au><au>Fitzgerald, Michael</au><au>Gill, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><ericid>EJ664542</ericid><atitle>Brief Report: A Case of Autism Associated with del(2)(q32.1q32.2) or (q32.2q32.3)</atitle><jtitle>Journal of autism and developmental disorders</jtitle><addtitle>J Autism Dev Disord</addtitle><date>2003-02-01</date><risdate>2003</risdate><volume>33</volume><issue>1</issue><spage>105</spage><epage>108</epage><pages>105-108</pages><issn>0162-3257</issn><eissn>1573-3432</eissn><coden>JADDDQ</coden><abstract>This paper reports a clinical case of autism with a deletion on chromosome 2 in a young male with high functioning autism. The deletion seems to correspond with regions emerging from linkage studies. The paper proposes this chromosomal region as a possible candidate region in the search for autism genes. (Contains references.) (Author/DB)</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>12708586</pmid><doi>10.1023/A:1022242807513</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0162-3257 |
ispartof | Journal of autism and developmental disorders, 2003-02, Vol.33 (1), p.105-108 |
issn | 0162-3257 1573-3432 |
language | eng |
recordid | cdi_proquest_miscellaneous_73200932 |
source | Applied Social Sciences Index & Abstracts (ASSIA); MEDLINE; Education Source; SpringerLink Journals - AutoHoldings |
subjects | Academic Achievement Adolescent Algorithms Autism Autistic Disorder - genetics Case Studies Chromosome Abnormalities Chromosomes, Human, Pair 2 - genetics Comprehension Cytogenetics - methods Departments Developmental Delays Elementary Education Etiology Evidence Gene Deletion Genetics Humans Imagination Interpersonal Relationship Karyotyping Learning Disabilities Male Males Mathematics Medical Evaluation Nonverbal Communication Performance Based Assessment Physical Development Physical Examinations Point Mutation - genetics Pregnancy Psychological Evaluation Research Needs Research Tools Special Needs Students Toilet Training |
title | Brief Report: A Case of Autism Associated with del(2)(q32.1q32.2) or (q32.2q32.3) |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T15%3A23%3A12IST&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=Brief%20Report:%20A%20Case%20of%20Autism%20Associated%20with%20del(2)(q32.1q32.2)%20or%20(q32.2q32.3)&rft.jtitle=Journal%20of%20autism%20and%20developmental%20disorders&rft.au=Gallagher,%20Louise&rft.date=2003-02-01&rft.volume=33&rft.issue=1&rft.spage=105&rft.epage=108&rft.pages=105-108&rft.issn=0162-3257&rft.eissn=1573-3432&rft.coden=JADDDQ&rft_id=info:doi/10.1023/A:1022242807513&rft_dat=%3Cproquest_pubme%3E977900931%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=205299357&rft_id=info:pmid/12708586&rft_ericid=EJ664542&rfr_iscdi=true |