Mutation Screening of Charcot-Marie-Tooth Patients in Poland

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Annals of the New York Academy of Sciences 1999-10, Vol.883 (1), p.493-496
Hauptverfasser: KOCHAŃSKI, A., TIMMERMAN, V., JEDRZEJOWSKA, H., RYNIEWICZ, B., LÖFGREN, A., De VRIENDT, E., VAN BROECKHOVEN, C., LATOS-BIELEŃSKA, A., HAUSMANOWA-PETRUSEWICZ, I.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 496
container_issue 1
container_start_page 493
container_title Annals of the New York Academy of Sciences
container_volume 883
creator KOCHAŃSKI, A.
TIMMERMAN, V.
JEDRZEJOWSKA, H.
RYNIEWICZ, B.
LÖFGREN, A.
De VRIENDT, E.
VAN BROECKHOVEN, C.
LATOS-BIELEŃSKA, A.
HAUSMANOWA-PETRUSEWICZ, I.
description
doi_str_mv 10.1111/j.1749-6632.1999.tb08619.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69336939</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1958539123</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3003-8caa9d42125388f7bde1ed9cf3a23a263012ec62d42d661101eb557c7f1c17c03</originalsourceid><addsrcrecordid>eNqVkF1LIzEUhoO4rF13_4IMXog3M5uTdPIhgkhZq2Bd0YroTUgzGZ3aTjSZYvvvzTCleCUYEnKR57x5eRDaB5xBXH-nGfC-TBmjJAMpZdZMsGAgs-UW6m2etlEPY85TIQndQb9CmGIMRPT5T7QDOBeMCNJDx6NFo5vK1cmt8dbWVf2UuDIZPGtvXJOOtK9sOnaueU6uI2frJiRVnVy7ma6L3-hHqWfB_lnfu-ju7N94cJ5e_h9eDE4vU0MxpqkwWsuiT4DkVIiSTwoLtpCmpJrEzWjsZQ0jESkYA8BgJ3nODS_BADeY7qKDLvfVu7eFDY2aV8HYWexg3SIoJimNR0bw8EsQZC5yKoHQiB51qPEuBG9L9eqrufYrBVi1mtVUtS5V61K1mtVas1rG4b31P4vJ3BafRjuvETjpgPdqZlffiFZXD6e3fdn2S7uEKjR2uUnQ_kUxTnmu7q-GSt6I0fgR52pIPwBaSpsc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1958539123</pqid></control><display><type>article</type><title>Mutation Screening of Charcot-Marie-Tooth Patients in Poland</title><source>Wiley Online Library - AutoHoldings Journals</source><source>MEDLINE</source><creator>KOCHAŃSKI, A. ; TIMMERMAN, V. ; JEDRZEJOWSKA, H. ; RYNIEWICZ, B. ; LÖFGREN, A. ; De VRIENDT, E. ; VAN BROECKHOVEN, C. ; LATOS-BIELEŃSKA, A. ; HAUSMANOWA-PETRUSEWICZ, I.</creator><creatorcontrib>KOCHAŃSKI, A. ; TIMMERMAN, V. ; JEDRZEJOWSKA, H. ; RYNIEWICZ, B. ; LÖFGREN, A. ; De VRIENDT, E. ; VAN BROECKHOVEN, C. ; LATOS-BIELEŃSKA, A. ; HAUSMANOWA-PETRUSEWICZ, I.</creatorcontrib><identifier>ISSN: 0077-8923</identifier><identifier>EISSN: 1749-6632</identifier><identifier>DOI: 10.1111/j.1749-6632.1999.tb08619.x</identifier><identifier>PMID: 10586282</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Charcot-Marie-Tooth Disease - diagnosis ; Charcot-Marie-Tooth Disease - genetics ; Chromosome Mapping ; Chromosomes, Human, Pair 17 ; Connexins - genetics ; Female ; Gap Junction beta-1 Protein ; Genetic Markers ; Genetic Testing ; Humans ; Male ; Myelin P0 Protein - genetics ; Myelin Proteins - genetics ; Pedigree ; Poland ; Polymorphism, Restriction Fragment Length</subject><ispartof>Annals of the New York Academy of Sciences, 1999-10, Vol.883 (1), p.493-496</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3003-8caa9d42125388f7bde1ed9cf3a23a263012ec62d42d661101eb557c7f1c17c03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1749-6632.1999.tb08619.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1749-6632.1999.tb08619.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,782,786,1419,27931,27932,45581,45582</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10586282$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KOCHAŃSKI, A.</creatorcontrib><creatorcontrib>TIMMERMAN, V.</creatorcontrib><creatorcontrib>JEDRZEJOWSKA, H.</creatorcontrib><creatorcontrib>RYNIEWICZ, B.</creatorcontrib><creatorcontrib>LÖFGREN, A.</creatorcontrib><creatorcontrib>De VRIENDT, E.</creatorcontrib><creatorcontrib>VAN BROECKHOVEN, C.</creatorcontrib><creatorcontrib>LATOS-BIELEŃSKA, A.</creatorcontrib><creatorcontrib>HAUSMANOWA-PETRUSEWICZ, I.</creatorcontrib><title>Mutation Screening of Charcot-Marie-Tooth Patients in Poland</title><title>Annals of the New York Academy of Sciences</title><addtitle>Ann N Y Acad Sci</addtitle><subject>Charcot-Marie-Tooth Disease - diagnosis</subject><subject>Charcot-Marie-Tooth Disease - genetics</subject><subject>Chromosome Mapping</subject><subject>Chromosomes, Human, Pair 17</subject><subject>Connexins - genetics</subject><subject>Female</subject><subject>Gap Junction beta-1 Protein</subject><subject>Genetic Markers</subject><subject>Genetic Testing</subject><subject>Humans</subject><subject>Male</subject><subject>Myelin P0 Protein - genetics</subject><subject>Myelin Proteins - genetics</subject><subject>Pedigree</subject><subject>Poland</subject><subject>Polymorphism, Restriction Fragment Length</subject><issn>0077-8923</issn><issn>1749-6632</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkF1LIzEUhoO4rF13_4IMXog3M5uTdPIhgkhZq2Bd0YroTUgzGZ3aTjSZYvvvzTCleCUYEnKR57x5eRDaB5xBXH-nGfC-TBmjJAMpZdZMsGAgs-UW6m2etlEPY85TIQndQb9CmGIMRPT5T7QDOBeMCNJDx6NFo5vK1cmt8dbWVf2UuDIZPGtvXJOOtK9sOnaueU6uI2frJiRVnVy7ma6L3-hHqWfB_lnfu-ju7N94cJ5e_h9eDE4vU0MxpqkwWsuiT4DkVIiSTwoLtpCmpJrEzWjsZQ0jESkYA8BgJ3nODS_BADeY7qKDLvfVu7eFDY2aV8HYWexg3SIoJimNR0bw8EsQZC5yKoHQiB51qPEuBG9L9eqrufYrBVi1mtVUtS5V61K1mtVas1rG4b31P4vJ3BafRjuvETjpgPdqZlffiFZXD6e3fdn2S7uEKjR2uUnQ_kUxTnmu7q-GSt6I0fgR52pIPwBaSpsc</recordid><startdate>199910</startdate><enddate>199910</enddate><creator>KOCHAŃSKI, A.</creator><creator>TIMMERMAN, V.</creator><creator>JEDRZEJOWSKA, H.</creator><creator>RYNIEWICZ, B.</creator><creator>LÖFGREN, A.</creator><creator>De VRIENDT, E.</creator><creator>VAN BROECKHOVEN, C.</creator><creator>LATOS-BIELEŃSKA, A.</creator><creator>HAUSMANOWA-PETRUSEWICZ, I.</creator><general>Blackwell Publishing Ltd</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><scope>7X8</scope></search><sort><creationdate>199910</creationdate><title>Mutation Screening of Charcot-Marie-Tooth Patients in Poland</title><author>KOCHAŃSKI, A. ; TIMMERMAN, V. ; JEDRZEJOWSKA, H. ; RYNIEWICZ, B. ; LÖFGREN, A. ; De VRIENDT, E. ; VAN BROECKHOVEN, C. ; LATOS-BIELEŃSKA, A. ; HAUSMANOWA-PETRUSEWICZ, I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3003-8caa9d42125388f7bde1ed9cf3a23a263012ec62d42d661101eb557c7f1c17c03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Charcot-Marie-Tooth Disease - diagnosis</topic><topic>Charcot-Marie-Tooth Disease - genetics</topic><topic>Chromosome Mapping</topic><topic>Chromosomes, Human, Pair 17</topic><topic>Connexins - genetics</topic><topic>Female</topic><topic>Gap Junction beta-1 Protein</topic><topic>Genetic Markers</topic><topic>Genetic Testing</topic><topic>Humans</topic><topic>Male</topic><topic>Myelin P0 Protein - genetics</topic><topic>Myelin Proteins - genetics</topic><topic>Pedigree</topic><topic>Poland</topic><topic>Polymorphism, Restriction Fragment Length</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KOCHAŃSKI, A.</creatorcontrib><creatorcontrib>TIMMERMAN, V.</creatorcontrib><creatorcontrib>JEDRZEJOWSKA, H.</creatorcontrib><creatorcontrib>RYNIEWICZ, B.</creatorcontrib><creatorcontrib>LÖFGREN, A.</creatorcontrib><creatorcontrib>De VRIENDT, E.</creatorcontrib><creatorcontrib>VAN BROECKHOVEN, C.</creatorcontrib><creatorcontrib>LATOS-BIELEŃSKA, A.</creatorcontrib><creatorcontrib>HAUSMANOWA-PETRUSEWICZ, I.</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><collection>MEDLINE - Academic</collection><jtitle>Annals of the New York Academy of Sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KOCHAŃSKI, A.</au><au>TIMMERMAN, V.</au><au>JEDRZEJOWSKA, H.</au><au>RYNIEWICZ, B.</au><au>LÖFGREN, A.</au><au>De VRIENDT, E.</au><au>VAN BROECKHOVEN, C.</au><au>LATOS-BIELEŃSKA, A.</au><au>HAUSMANOWA-PETRUSEWICZ, I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mutation Screening of Charcot-Marie-Tooth Patients in Poland</atitle><jtitle>Annals of the New York Academy of Sciences</jtitle><addtitle>Ann N Y Acad Sci</addtitle><date>1999-10</date><risdate>1999</risdate><volume>883</volume><issue>1</issue><spage>493</spage><epage>496</epage><pages>493-496</pages><issn>0077-8923</issn><eissn>1749-6632</eissn><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>10586282</pmid><doi>10.1111/j.1749-6632.1999.tb08619.x</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0077-8923
ispartof Annals of the New York Academy of Sciences, 1999-10, Vol.883 (1), p.493-496
issn 0077-8923
1749-6632
language eng
recordid cdi_proquest_miscellaneous_69336939
source Wiley Online Library - AutoHoldings Journals; MEDLINE
subjects Charcot-Marie-Tooth Disease - diagnosis
Charcot-Marie-Tooth Disease - genetics
Chromosome Mapping
Chromosomes, Human, Pair 17
Connexins - genetics
Female
Gap Junction beta-1 Protein
Genetic Markers
Genetic Testing
Humans
Male
Myelin P0 Protein - genetics
Myelin Proteins - genetics
Pedigree
Poland
Polymorphism, Restriction Fragment Length
title Mutation Screening of Charcot-Marie-Tooth Patients in Poland
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-09T09%3A47%3A33IST&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=Mutation%20Screening%20of%20Charcot-Marie-Tooth%20Patients%20in%20Poland&rft.jtitle=Annals%20of%20the%20New%20York%20Academy%20of%20Sciences&rft.au=KOCHA%C5%83SKI,%20A.&rft.date=1999-10&rft.volume=883&rft.issue=1&rft.spage=493&rft.epage=496&rft.pages=493-496&rft.issn=0077-8923&rft.eissn=1749-6632&rft_id=info:doi/10.1111/j.1749-6632.1999.tb08619.x&rft_dat=%3Cproquest_cross%3E1958539123%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=1958539123&rft_id=info:pmid/10586282&rfr_iscdi=true