Nonrandom X-Chromosome Inactivation in Hemopoietic Cells from Carriers of Dyskeratosis Congenita
Gespeichert in:
Veröffentlicht in: | American journal of human genetics 1997-08, Vol.61 (2), p.458-461 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 461 |
---|---|
container_issue | 2 |
container_start_page | 458 |
container_title | American journal of human genetics |
container_volume | 61 |
creator | FERRARIS, ANNA MARIA FORNI, GIAN LUCA MANGERINI, ROSA GAETANI, GIAN FRANCO |
description | |
doi_str_mv | 10.1016/S0002-9297(07)64075-0 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1715903</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0002929707640750</els_id><sourcerecordid>79312077</sourcerecordid><originalsourceid>FETCH-LOGICAL-c462t-9843085c87feee1440513c0d34ca268fe5396c1bfe05a9c2fe0030783ed9ad5f3</originalsourceid><addsrcrecordid>eNqFUU1v1DAQtRCobFt-QiWfEBwC4ziOkwsIBUorVeVAkbgZ15m0ho1na3tX6r-v212t4MRpDu9jZt5j7ETAOwGiff8dAOqqr3v9BvTbtgGtKnjGFkJJXbUtqOdssae8ZIcp_QYQogN5wA56KYRWzYL9uqQQbRhp5j-r4TbSTIlm5OfBuuw3NnsK3Ad-hjOtyGP2jg-4XCY-FS4fbIweY-I08c_36Q9Gmyn5xAcKNxh8tsfsxWSXCV_t5hH7cfrlajirLr59PR8-XVSuaetc9V0joVOu0xMiiqYBJaSDUTbO1m03oZJ968T1hKBs7-oyQYLuJI69HdUkj9iHre9qfT3j6DDkaJdmFf1s470h682_SPC35oY2RmihepDF4PXOINLdGlM2s0-uvGoD0joZXTKrQetCVFuii5RSxGm_RIB5rMY8VWMeczegzVM1Boru5O8L96pdFwX_uMWxxLQpqZrkPAaHo4_oshnJ_2fDA1q2oG0</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>79312077</pqid></control><display><type>article</type><title>Nonrandom X-Chromosome Inactivation in Hemopoietic Cells from Carriers of Dyskeratosis Congenita</title><source>MEDLINE</source><source>Cell Press Free Archives</source><source>Access via ScienceDirect (Elsevier)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>FERRARIS, ANNA MARIA ; FORNI, GIAN LUCA ; MANGERINI, ROSA ; GAETANI, GIAN FRANCO</creator><creatorcontrib>FERRARIS, ANNA MARIA ; FORNI, GIAN LUCA ; MANGERINI, ROSA ; GAETANI, GIAN FRANCO</creatorcontrib><identifier>ISSN: 0002-9297</identifier><identifier>EISSN: 1537-6605</identifier><identifier>DOI: 10.1016/S0002-9297(07)64075-0</identifier><identifier>PMID: 9311754</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Alleles ; Dosage Compensation, Genetic ; Ectodermal Dysplasia - blood ; Ectodermal Dysplasia - genetics ; Female ; Genetic Carrier Screening ; Hematopoietic Stem Cells - cytology ; Humans ; Letter ; Male ; Pedigree ; Selection, Genetic ; X Chromosome - genetics</subject><ispartof>American journal of human genetics, 1997-08, Vol.61 (2), p.458-461</ispartof><rights>1997 The American Society of Human Genetics</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-9843085c87feee1440513c0d34ca268fe5396c1bfe05a9c2fe0030783ed9ad5f3</citedby><cites>FETCH-LOGICAL-c462t-9843085c87feee1440513c0d34ca268fe5396c1bfe05a9c2fe0030783ed9ad5f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1715903/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0002-9297(07)64075-0$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3550,27924,27925,45995,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9311754$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>FERRARIS, ANNA MARIA</creatorcontrib><creatorcontrib>FORNI, GIAN LUCA</creatorcontrib><creatorcontrib>MANGERINI, ROSA</creatorcontrib><creatorcontrib>GAETANI, GIAN FRANCO</creatorcontrib><title>Nonrandom X-Chromosome Inactivation in Hemopoietic Cells from Carriers of Dyskeratosis Congenita</title><title>American journal of human genetics</title><addtitle>Am J Hum Genet</addtitle><subject>Alleles</subject><subject>Dosage Compensation, Genetic</subject><subject>Ectodermal Dysplasia - blood</subject><subject>Ectodermal Dysplasia - genetics</subject><subject>Female</subject><subject>Genetic Carrier Screening</subject><subject>Hematopoietic Stem Cells - cytology</subject><subject>Humans</subject><subject>Letter</subject><subject>Male</subject><subject>Pedigree</subject><subject>Selection, Genetic</subject><subject>X Chromosome - genetics</subject><issn>0002-9297</issn><issn>1537-6605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUU1v1DAQtRCobFt-QiWfEBwC4ziOkwsIBUorVeVAkbgZ15m0ho1na3tX6r-v212t4MRpDu9jZt5j7ETAOwGiff8dAOqqr3v9BvTbtgGtKnjGFkJJXbUtqOdssae8ZIcp_QYQogN5wA56KYRWzYL9uqQQbRhp5j-r4TbSTIlm5OfBuuw3NnsK3Ad-hjOtyGP2jg-4XCY-FS4fbIweY-I08c_36Q9Gmyn5xAcKNxh8tsfsxWSXCV_t5hH7cfrlajirLr59PR8-XVSuaetc9V0joVOu0xMiiqYBJaSDUTbO1m03oZJ968T1hKBs7-oyQYLuJI69HdUkj9iHre9qfT3j6DDkaJdmFf1s470h682_SPC35oY2RmihepDF4PXOINLdGlM2s0-uvGoD0joZXTKrQetCVFuii5RSxGm_RIB5rMY8VWMeczegzVM1Boru5O8L96pdFwX_uMWxxLQpqZrkPAaHo4_oshnJ_2fDA1q2oG0</recordid><startdate>19970801</startdate><enddate>19970801</enddate><creator>FERRARIS, ANNA MARIA</creator><creator>FORNI, GIAN LUCA</creator><creator>MANGERINI, ROSA</creator><creator>GAETANI, GIAN FRANCO</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</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><scope>5PM</scope></search><sort><creationdate>19970801</creationdate><title>Nonrandom X-Chromosome Inactivation in Hemopoietic Cells from Carriers of Dyskeratosis Congenita</title><author>FERRARIS, ANNA MARIA ; FORNI, GIAN LUCA ; MANGERINI, ROSA ; GAETANI, GIAN FRANCO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-9843085c87feee1440513c0d34ca268fe5396c1bfe05a9c2fe0030783ed9ad5f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Alleles</topic><topic>Dosage Compensation, Genetic</topic><topic>Ectodermal Dysplasia - blood</topic><topic>Ectodermal Dysplasia - genetics</topic><topic>Female</topic><topic>Genetic Carrier Screening</topic><topic>Hematopoietic Stem Cells - cytology</topic><topic>Humans</topic><topic>Letter</topic><topic>Male</topic><topic>Pedigree</topic><topic>Selection, Genetic</topic><topic>X Chromosome - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FERRARIS, ANNA MARIA</creatorcontrib><creatorcontrib>FORNI, GIAN LUCA</creatorcontrib><creatorcontrib>MANGERINI, ROSA</creatorcontrib><creatorcontrib>GAETANI, GIAN FRANCO</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of human genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FERRARIS, ANNA MARIA</au><au>FORNI, GIAN LUCA</au><au>MANGERINI, ROSA</au><au>GAETANI, GIAN FRANCO</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nonrandom X-Chromosome Inactivation in Hemopoietic Cells from Carriers of Dyskeratosis Congenita</atitle><jtitle>American journal of human genetics</jtitle><addtitle>Am J Hum Genet</addtitle><date>1997-08-01</date><risdate>1997</risdate><volume>61</volume><issue>2</issue><spage>458</spage><epage>461</epage><pages>458-461</pages><issn>0002-9297</issn><eissn>1537-6605</eissn><cop>United States</cop><pub>Elsevier Inc</pub><pmid>9311754</pmid><doi>10.1016/S0002-9297(07)64075-0</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0002-9297 |
ispartof | American journal of human genetics, 1997-08, Vol.61 (2), p.458-461 |
issn | 0002-9297 1537-6605 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1715903 |
source | MEDLINE; Cell Press Free Archives; Access via ScienceDirect (Elsevier); EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Alleles Dosage Compensation, Genetic Ectodermal Dysplasia - blood Ectodermal Dysplasia - genetics Female Genetic Carrier Screening Hematopoietic Stem Cells - cytology Humans Letter Male Pedigree Selection, Genetic X Chromosome - genetics |
title | Nonrandom X-Chromosome Inactivation in Hemopoietic Cells from Carriers of Dyskeratosis Congenita |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-22T12%3A28%3A01IST&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=Nonrandom%20X-Chromosome%20Inactivation%20in%20Hemopoietic%20Cells%20from%20Carriers%20of%20Dyskeratosis%20Congenita&rft.jtitle=American%20journal%20of%20human%20genetics&rft.au=FERRARIS,%20ANNA%20MARIA&rft.date=1997-08-01&rft.volume=61&rft.issue=2&rft.spage=458&rft.epage=461&rft.pages=458-461&rft.issn=0002-9297&rft.eissn=1537-6605&rft_id=info:doi/10.1016/S0002-9297(07)64075-0&rft_dat=%3Cproquest_pubme%3E79312077%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=79312077&rft_id=info:pmid/9311754&rft_els_id=S0002929707640750&rfr_iscdi=true |