Microdissection – a precise method to disclose the parental origin of supernumerary marker chromosomes
Gespeichert in:
| Veröffentlicht in: | Annales de génétique 2000-04, Vol.43 (2), p.109-110 |
|---|---|
| Hauptverfasser: | , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 110 |
|---|---|
| container_issue | 2 |
| container_start_page | 109 |
| container_title | Annales de génétique |
| container_volume | 43 |
| creator | Friedrich, Ursula Bugge, Merete Houman, Mette Friis Henriksen, Karen Brøndum-Nielsen, Karen |
| description | |
| doi_str_mv | 10.1016/S0003-3995(00)01015-7 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72280059</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0003399500010157</els_id><sourcerecordid>72280059</sourcerecordid><originalsourceid>FETCH-LOGICAL-c390t-fa6df60a75f98cc1ba2f72727cbea53010e0b7ad1cc894cb897f21b77fcecd223</originalsourceid><addsrcrecordid>eNqFkMFO3DAQhn2ggmXhEUA-VFU5BMbJZh2fKoSgrQTiUDhbzmTMmiZxaieVuPEOvCFPUi-7arlVPlgefeP552PsSMCpALE8-wEARVYoVX4GOIFUKzO5w2Z_y3tsP8bH9CxhudhlewKUqhblYsZWNw6Db1yMhKPzPX99fuGGD4HQReIdjSvf8NHzhGDrU2lcER9MoH40LffBPbiee8vjNFDop46CCU-8M-EnBY6r4DsffUfxgH2wpo10uL3n7P7q8u7iW3Z9-_X7xfl1hoWCMbNm2dglGFlaVSGK2uRW5ulgTaYs0m4EtTSNQKzUAutKSZuLWkqLhE2eF3P2afPvEPyvieKou5Sc2tb05KeoZZ5XyYNKYLkB0_4xBrJ6CC7lftIC9FqrftOq1_40gH7TqmXqO94OmOqOmnddG6cJ-LgFTETT2mD65PIfV4IQYo192WCUbPx2FHRERz1S45L8UTfe_SfJHwyLmZs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>72280059</pqid></control><display><type>article</type><title>Microdissection – a precise method to disclose the parental origin of supernumerary marker chromosomes</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Friedrich, Ursula ; Bugge, Merete ; Houman, Mette ; Friis Henriksen, Karen ; Brøndum-Nielsen, Karen</creator><creatorcontrib>Friedrich, Ursula ; Bugge, Merete ; Houman, Mette ; Friis Henriksen, Karen ; Brøndum-Nielsen, Karen</creatorcontrib><identifier>ISSN: 0003-3995</identifier><identifier>DOI: 10.1016/S0003-3995(00)01015-7</identifier><identifier>PMID: 10998454</identifier><identifier>CODEN: AGTQAH</identifier><language>eng</language><publisher>Paris: Elsevier SAS</publisher><subject>Biological and medical sciences ; Chromosome Aberrations ; Chromosome Banding - methods ; Chromosomes, Human, Pair 18 - genetics ; Female ; Genetic Markers ; Humans ; isochromosome 18p ; Male ; Medical genetics ; Medical sciences ; microdissection ; Microsatellite Repeats - genetics ; parental origin ; Polymerase Chain Reaction - methods ; Polymorphism, Genetic</subject><ispartof>Annales de génétique, 2000-04, Vol.43 (2), p.109-110</ispartof><rights>2000 Éditions scientifiques et médicales Elsevier SAS</rights><rights>2000 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-fa6df60a75f98cc1ba2f72727cbea53010e0b7ad1cc894cb897f21b77fcecd223</citedby><cites>FETCH-LOGICAL-c390t-fa6df60a75f98cc1ba2f72727cbea53010e0b7ad1cc894cb897f21b77fcecd223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1501114$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10998454$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Friedrich, Ursula</creatorcontrib><creatorcontrib>Bugge, Merete</creatorcontrib><creatorcontrib>Houman, Mette</creatorcontrib><creatorcontrib>Friis Henriksen, Karen</creatorcontrib><creatorcontrib>Brøndum-Nielsen, Karen</creatorcontrib><title>Microdissection – a precise method to disclose the parental origin of supernumerary marker chromosomes</title><title>Annales de génétique</title><addtitle>Ann Genet</addtitle><subject>Biological and medical sciences</subject><subject>Chromosome Aberrations</subject><subject>Chromosome Banding - methods</subject><subject>Chromosomes, Human, Pair 18 - genetics</subject><subject>Female</subject><subject>Genetic Markers</subject><subject>Humans</subject><subject>isochromosome 18p</subject><subject>Male</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>microdissection</subject><subject>Microsatellite Repeats - genetics</subject><subject>parental origin</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Polymorphism, Genetic</subject><issn>0003-3995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMFO3DAQhn2ggmXhEUA-VFU5BMbJZh2fKoSgrQTiUDhbzmTMmiZxaieVuPEOvCFPUi-7arlVPlgefeP552PsSMCpALE8-wEARVYoVX4GOIFUKzO5w2Z_y3tsP8bH9CxhudhlewKUqhblYsZWNw6Db1yMhKPzPX99fuGGD4HQReIdjSvf8NHzhGDrU2lcER9MoH40LffBPbiee8vjNFDop46CCU-8M-EnBY6r4DsffUfxgH2wpo10uL3n7P7q8u7iW3Z9-_X7xfl1hoWCMbNm2dglGFlaVSGK2uRW5ulgTaYs0m4EtTSNQKzUAutKSZuLWkqLhE2eF3P2afPvEPyvieKou5Sc2tb05KeoZZ5XyYNKYLkB0_4xBrJ6CC7lftIC9FqrftOq1_40gH7TqmXqO94OmOqOmnddG6cJ-LgFTETT2mD65PIfV4IQYo192WCUbPx2FHRERz1S45L8UTfe_SfJHwyLmZs</recordid><startdate>20000401</startdate><enddate>20000401</enddate><creator>Friedrich, Ursula</creator><creator>Bugge, Merete</creator><creator>Houman, Mette</creator><creator>Friis Henriksen, Karen</creator><creator>Brøndum-Nielsen, Karen</creator><general>Elsevier SAS</general><general>Société d'édition de l'association d'enseignement médical des hôpitaux de Paris</general><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>7X8</scope></search><sort><creationdate>20000401</creationdate><title>Microdissection – a precise method to disclose the parental origin of supernumerary marker chromosomes</title><author>Friedrich, Ursula ; Bugge, Merete ; Houman, Mette ; Friis Henriksen, Karen ; Brøndum-Nielsen, Karen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-fa6df60a75f98cc1ba2f72727cbea53010e0b7ad1cc894cb897f21b77fcecd223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Biological and medical sciences</topic><topic>Chromosome Aberrations</topic><topic>Chromosome Banding - methods</topic><topic>Chromosomes, Human, Pair 18 - genetics</topic><topic>Female</topic><topic>Genetic Markers</topic><topic>Humans</topic><topic>isochromosome 18p</topic><topic>Male</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>microdissection</topic><topic>Microsatellite Repeats - genetics</topic><topic>parental origin</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Polymorphism, Genetic</topic><toplevel>online_resources</toplevel><creatorcontrib>Friedrich, Ursula</creatorcontrib><creatorcontrib>Bugge, Merete</creatorcontrib><creatorcontrib>Houman, Mette</creatorcontrib><creatorcontrib>Friis Henriksen, Karen</creatorcontrib><creatorcontrib>Brøndum-Nielsen, Karen</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Annales de génétique</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Friedrich, Ursula</au><au>Bugge, Merete</au><au>Houman, Mette</au><au>Friis Henriksen, Karen</au><au>Brøndum-Nielsen, Karen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microdissection – a precise method to disclose the parental origin of supernumerary marker chromosomes</atitle><jtitle>Annales de génétique</jtitle><addtitle>Ann Genet</addtitle><date>2000-04-01</date><risdate>2000</risdate><volume>43</volume><issue>2</issue><spage>109</spage><epage>110</epage><pages>109-110</pages><issn>0003-3995</issn><coden>AGTQAH</coden><cop>Paris</cop><pub>Elsevier SAS</pub><pmid>10998454</pmid><doi>10.1016/S0003-3995(00)01015-7</doi><tpages>2</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0003-3995 |
| ispartof | Annales de génétique, 2000-04, Vol.43 (2), p.109-110 |
| issn | 0003-3995 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_72280059 |
| source | MEDLINE; Alma/SFX Local Collection |
| subjects | Biological and medical sciences Chromosome Aberrations Chromosome Banding - methods Chromosomes, Human, Pair 18 - genetics Female Genetic Markers Humans isochromosome 18p Male Medical genetics Medical sciences microdissection Microsatellite Repeats - genetics parental origin Polymerase Chain Reaction - methods Polymorphism, Genetic |
| title | Microdissection – a precise method to disclose the parental origin of supernumerary marker chromosomes |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T07%3A13%3A14IST&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=Microdissection%20%E2%80%93%20a%20precise%20method%20to%20disclose%20the%20parental%20origin%20of%20supernumerary%20marker%20chromosomes&rft.jtitle=Annales%20de%20g%C3%A9n%C3%A9tique&rft.au=Friedrich,%20Ursula&rft.date=2000-04-01&rft.volume=43&rft.issue=2&rft.spage=109&rft.epage=110&rft.pages=109-110&rft.issn=0003-3995&rft.coden=AGTQAH&rft_id=info:doi/10.1016/S0003-3995(00)01015-7&rft_dat=%3Cproquest_cross%3E72280059%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=72280059&rft_id=info:pmid/10998454&rft_els_id=S0003399500010157&rfr_iscdi=true |