RFLP FOR LINKAGE ANALYSIS OF FRAGILE X SYNDROME

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Lancet (British edition) 1987-01, Vol.329 (8527), p.280-280
Hauptverfasser: Ted Brown, W., Wu, Ye, Gross, AnneC, Chan, ColinB, Dobkin, CarlS, Jenkins, EdmundC
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 280
container_issue 8527
container_start_page 280
container_title The Lancet (British edition)
container_volume 329
creator Ted Brown, W.
Wu, Ye
Gross, AnneC
Chan, ColinB
Dobkin, CarlS
Jenkins, EdmundC
description
doi_str_mv 10.1016/S0140-6736(87)90103-6
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_77382578</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0140673687901036</els_id><sourcerecordid>77382578</sourcerecordid><originalsourceid>FETCH-LOGICAL-c430t-94bab20556d211c2e060fed22a014d2f7cee93bdd877881cdc6515c869f65b583</originalsourceid><addsrcrecordid>eNqFkEtLw0AUhQdRaq3-hEJWoovYmUnmkZWEmtRgbCRRaFdDMnMDkb7MtIL_3vSBW1d3cc65594PoSHBDwQTPiow8bHLhcfvpLgPMMGey89Qn_jCd5kvZueo_2e5RFfWfmKMfY5ZD_WolF2A9tEoj9M3J85yJ02mL-EkcsJpmM6LpHCy2InzcJKkkTNzivn0Kc9eo2t0UZcLCzenOUAfcfQ-fnbTbJKMw9TVvoe3buBXZUUxY9xQQjQFzHENhtKyO8nQWmiAwKuMkUJISbTRnBGmJQ9qziomvQG6Pe7dtOuvHditWjZWw2JRrmC9s0oIT1Im9kZ2NOp2bW0Ltdq0zbJsfxTBag9KHUCpPQUlhTqAUrzLDU8Fu2oJ5i91ItPpj0cdui-_G2iV1Q2sNJimBb1VZt380_ALJW5xrg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>77382578</pqid></control><display><type>article</type><title>RFLP FOR LINKAGE ANALYSIS OF FRAGILE X SYNDROME</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Ted Brown, W. ; Wu, Ye ; Gross, AnneC ; Chan, ColinB ; Dobkin, CarlS ; Jenkins, EdmundC</creator><creatorcontrib>Ted Brown, W. ; Wu, Ye ; Gross, AnneC ; Chan, ColinB ; Dobkin, CarlS ; Jenkins, EdmundC</creatorcontrib><identifier>ISSN: 0140-6736</identifier><identifier>EISSN: 1474-547X</identifier><identifier>DOI: 10.1016/S0140-6736(87)90103-6</identifier><identifier>PMID: 2880102</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Female ; Fragile X Syndrome - genetics ; Genetic Linkage ; Humans ; Male ; Polymorphism, Genetic ; Polymorphism, Restriction Fragment Length ; Recombination, Genetic ; Sex Chromosome Aberrations - genetics ; Software</subject><ispartof>The Lancet (British edition), 1987-01, Vol.329 (8527), p.280-280</ispartof><rights>1987</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c430t-94bab20556d211c2e060fed22a014d2f7cee93bdd877881cdc6515c869f65b583</citedby><cites>FETCH-LOGICAL-c430t-94bab20556d211c2e060fed22a014d2f7cee93bdd877881cdc6515c869f65b583</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0140-6736(87)90103-6$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2880102$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ted Brown, W.</creatorcontrib><creatorcontrib>Wu, Ye</creatorcontrib><creatorcontrib>Gross, AnneC</creatorcontrib><creatorcontrib>Chan, ColinB</creatorcontrib><creatorcontrib>Dobkin, CarlS</creatorcontrib><creatorcontrib>Jenkins, EdmundC</creatorcontrib><title>RFLP FOR LINKAGE ANALYSIS OF FRAGILE X SYNDROME</title><title>The Lancet (British edition)</title><addtitle>Lancet</addtitle><subject>Female</subject><subject>Fragile X Syndrome - genetics</subject><subject>Genetic Linkage</subject><subject>Humans</subject><subject>Male</subject><subject>Polymorphism, Genetic</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>Recombination, Genetic</subject><subject>Sex Chromosome Aberrations - genetics</subject><subject>Software</subject><issn>0140-6736</issn><issn>1474-547X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLw0AUhQdRaq3-hEJWoovYmUnmkZWEmtRgbCRRaFdDMnMDkb7MtIL_3vSBW1d3cc65594PoSHBDwQTPiow8bHLhcfvpLgPMMGey89Qn_jCd5kvZueo_2e5RFfWfmKMfY5ZD_WolF2A9tEoj9M3J85yJ02mL-EkcsJpmM6LpHCy2InzcJKkkTNzivn0Kc9eo2t0UZcLCzenOUAfcfQ-fnbTbJKMw9TVvoe3buBXZUUxY9xQQjQFzHENhtKyO8nQWmiAwKuMkUJISbTRnBGmJQ9qziomvQG6Pe7dtOuvHditWjZWw2JRrmC9s0oIT1Im9kZ2NOp2bW0Ltdq0zbJsfxTBag9KHUCpPQUlhTqAUrzLDU8Fu2oJ5i91ItPpj0cdui-_G2iV1Q2sNJimBb1VZt380_ALJW5xrg</recordid><startdate>19870131</startdate><enddate>19870131</enddate><creator>Ted Brown, W.</creator><creator>Wu, Ye</creator><creator>Gross, AnneC</creator><creator>Chan, ColinB</creator><creator>Dobkin, CarlS</creator><creator>Jenkins, EdmundC</creator><general>Elsevier Ltd</general><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>19870131</creationdate><title>RFLP FOR LINKAGE ANALYSIS OF FRAGILE X SYNDROME</title><author>Ted Brown, W. ; Wu, Ye ; Gross, AnneC ; Chan, ColinB ; Dobkin, CarlS ; Jenkins, EdmundC</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-94bab20556d211c2e060fed22a014d2f7cee93bdd877881cdc6515c869f65b583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Female</topic><topic>Fragile X Syndrome - genetics</topic><topic>Genetic Linkage</topic><topic>Humans</topic><topic>Male</topic><topic>Polymorphism, Genetic</topic><topic>Polymorphism, Restriction Fragment Length</topic><topic>Recombination, Genetic</topic><topic>Sex Chromosome Aberrations - genetics</topic><topic>Software</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ted Brown, W.</creatorcontrib><creatorcontrib>Wu, Ye</creatorcontrib><creatorcontrib>Gross, AnneC</creatorcontrib><creatorcontrib>Chan, ColinB</creatorcontrib><creatorcontrib>Dobkin, CarlS</creatorcontrib><creatorcontrib>Jenkins, EdmundC</creatorcontrib><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>The Lancet (British edition)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ted Brown, W.</au><au>Wu, Ye</au><au>Gross, AnneC</au><au>Chan, ColinB</au><au>Dobkin, CarlS</au><au>Jenkins, EdmundC</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>RFLP FOR LINKAGE ANALYSIS OF FRAGILE X SYNDROME</atitle><jtitle>The Lancet (British edition)</jtitle><addtitle>Lancet</addtitle><date>1987-01-31</date><risdate>1987</risdate><volume>329</volume><issue>8527</issue><spage>280</spage><epage>280</epage><pages>280-280</pages><issn>0140-6736</issn><eissn>1474-547X</eissn><cop>England</cop><pub>Elsevier Ltd</pub><pmid>2880102</pmid><doi>10.1016/S0140-6736(87)90103-6</doi><tpages>1</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0140-6736
ispartof The Lancet (British edition), 1987-01, Vol.329 (8527), p.280-280
issn 0140-6736
1474-547X
language eng
recordid cdi_proquest_miscellaneous_77382578
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Female
Fragile X Syndrome - genetics
Genetic Linkage
Humans
Male
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Recombination, Genetic
Sex Chromosome Aberrations - genetics
Software
title RFLP FOR LINKAGE ANALYSIS OF FRAGILE X SYNDROME
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T08%3A05%3A10IST&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=RFLP%20FOR%20LINKAGE%20ANALYSIS%20OF%20FRAGILE%20X%20SYNDROME&rft.jtitle=The%20Lancet%20(British%20edition)&rft.au=Ted%20Brown,%20W.&rft.date=1987-01-31&rft.volume=329&rft.issue=8527&rft.spage=280&rft.epage=280&rft.pages=280-280&rft.issn=0140-6736&rft.eissn=1474-547X&rft_id=info:doi/10.1016/S0140-6736(87)90103-6&rft_dat=%3Cproquest_cross%3E77382578%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=77382578&rft_id=info:pmid/2880102&rft_els_id=S0140673687901036&rfr_iscdi=true