Childhood bone marrow monosomy 7 syndrome: A familial disorder?

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of pediatrics 1985-10, Vol.107 (4), p.578-580
Hauptverfasser: Carroll, William L., Morgan, Rodman, Glader, Bertil E.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 580
container_issue 4
container_start_page 578
container_title The Journal of pediatrics
container_volume 107
creator Carroll, William L.
Morgan, Rodman
Glader, Bertil E.
description
doi_str_mv 10.1016/S0022-3476(85)80027-5
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_76394968</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022347685800275</els_id><sourcerecordid>76394968</sourcerecordid><originalsourceid>FETCH-LOGICAL-c389t-181ed06cf0216e8ae4dd7f87a2d37da54f8f9712ee1385dac92700bdcbbb07a3</originalsourceid><addsrcrecordid>eNqFkE9PwzAMxSMEGmPwESb1gBAcCk7TNimXaZr4J03iwO5RmrhaUNtAsoH27enWaldOlvWe_ewfIVMK9xRo_vABkCQxS3l-K7I70XU8zk7ImELB41wwdkrGR8s5uQjhEwCKFGBERkzkiYB0TGaLta3N2jkTla7FqFHeu9-oca0LrtlFPAq71njX4GM0jyrV2NqqOjI2OG_Qzy7JWaXqgFdDnZDV89Nq8Rov31_eFvNlrJkoNjEVFA3kuoKE5igUpsbwSnCVGMaNytJKVAWnCSJlIjNKFwkHKI0uyxK4YhNy06_98u57i2EjGxs01rVq0W2D5Dkr0qL7ekKy3qi9C8FjJb-87Z7aSQpyz00euMk9FCkyeeAms25uOgRsywbNcWoA1enXg66CVnXlVattONpEWmR9_Ky3Ycfix6KXQVtsNRrrUW-kcfafQ_4AcymJYg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>76394968</pqid></control><display><type>article</type><title>Childhood bone marrow monosomy 7 syndrome: A familial disorder?</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Carroll, William L. ; Morgan, Rodman ; Glader, Bertil E.</creator><creatorcontrib>Carroll, William L. ; Morgan, Rodman ; Glader, Bertil E.</creatorcontrib><identifier>ISSN: 0022-3476</identifier><identifier>EISSN: 1097-6833</identifier><identifier>DOI: 10.1016/S0022-3476(85)80027-5</identifier><identifier>PMID: 3862804</identifier><identifier>CODEN: JOPDAB</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Biological and medical sciences ; Child ; Chromosome Deletion ; Chromosomes, Human, 6-12 and X ; Female ; Hematologic and hematopoietic diseases ; Humans ; Infant ; Leukemia, Myeloid, Acute - genetics ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Male ; Medical sciences ; Monosomy ; Myeloproliferative Disorders - genetics</subject><ispartof>The Journal of pediatrics, 1985-10, Vol.107 (4), p.578-580</ispartof><rights>1985 The C. V. Mosby Company</rights><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-181ed06cf0216e8ae4dd7f87a2d37da54f8f9712ee1385dac92700bdcbbb07a3</citedby><cites>FETCH-LOGICAL-c389t-181ed06cf0216e8ae4dd7f87a2d37da54f8f9712ee1385dac92700bdcbbb07a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0022-3476(85)80027-5$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=8495968$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3862804$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Carroll, William L.</creatorcontrib><creatorcontrib>Morgan, Rodman</creatorcontrib><creatorcontrib>Glader, Bertil E.</creatorcontrib><title>Childhood bone marrow monosomy 7 syndrome: A familial disorder?</title><title>The Journal of pediatrics</title><addtitle>J Pediatr</addtitle><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Chromosome Deletion</subject><subject>Chromosomes, Human, 6-12 and X</subject><subject>Female</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Infant</subject><subject>Leukemia, Myeloid, Acute - genetics</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Monosomy</subject><subject>Myeloproliferative Disorders - genetics</subject><issn>0022-3476</issn><issn>1097-6833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE9PwzAMxSMEGmPwESb1gBAcCk7TNimXaZr4J03iwO5RmrhaUNtAsoH27enWaldOlvWe_ewfIVMK9xRo_vABkCQxS3l-K7I70XU8zk7ImELB41wwdkrGR8s5uQjhEwCKFGBERkzkiYB0TGaLta3N2jkTla7FqFHeu9-oca0LrtlFPAq71njX4GM0jyrV2NqqOjI2OG_Qzy7JWaXqgFdDnZDV89Nq8Rov31_eFvNlrJkoNjEVFA3kuoKE5igUpsbwSnCVGMaNytJKVAWnCSJlIjNKFwkHKI0uyxK4YhNy06_98u57i2EjGxs01rVq0W2D5Dkr0qL7ekKy3qi9C8FjJb-87Z7aSQpyz00euMk9FCkyeeAms25uOgRsywbNcWoA1enXg66CVnXlVattONpEWmR9_Ky3Ycfix6KXQVtsNRrrUW-kcfafQ_4AcymJYg</recordid><startdate>198510</startdate><enddate>198510</enddate><creator>Carroll, William L.</creator><creator>Morgan, Rodman</creator><creator>Glader, Bertil E.</creator><general>Mosby, Inc</general><general>Elsevier</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>198510</creationdate><title>Childhood bone marrow monosomy 7 syndrome: A familial disorder?</title><author>Carroll, William L. ; Morgan, Rodman ; Glader, Bertil E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-181ed06cf0216e8ae4dd7f87a2d37da54f8f9712ee1385dac92700bdcbbb07a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Chromosome Deletion</topic><topic>Chromosomes, Human, 6-12 and X</topic><topic>Female</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Infant</topic><topic>Leukemia, Myeloid, Acute - genetics</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Monosomy</topic><topic>Myeloproliferative Disorders - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carroll, William L.</creatorcontrib><creatorcontrib>Morgan, Rodman</creatorcontrib><creatorcontrib>Glader, Bertil E.</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>The Journal of pediatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carroll, William L.</au><au>Morgan, Rodman</au><au>Glader, Bertil E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Childhood bone marrow monosomy 7 syndrome: A familial disorder?</atitle><jtitle>The Journal of pediatrics</jtitle><addtitle>J Pediatr</addtitle><date>1985-10</date><risdate>1985</risdate><volume>107</volume><issue>4</issue><spage>578</spage><epage>580</epage><pages>578-580</pages><issn>0022-3476</issn><eissn>1097-6833</eissn><coden>JOPDAB</coden><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>3862804</pmid><doi>10.1016/S0022-3476(85)80027-5</doi><tpages>3</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0022-3476
ispartof The Journal of pediatrics, 1985-10, Vol.107 (4), p.578-580
issn 0022-3476
1097-6833
language eng
recordid cdi_proquest_miscellaneous_76394968
source MEDLINE; Elsevier ScienceDirect Journals
subjects Biological and medical sciences
Child
Chromosome Deletion
Chromosomes, Human, 6-12 and X
Female
Hematologic and hematopoietic diseases
Humans
Infant
Leukemia, Myeloid, Acute - genetics
Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
Male
Medical sciences
Monosomy
Myeloproliferative Disorders - genetics
title Childhood bone marrow monosomy 7 syndrome: A familial disorder?
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-23T07%3A21%3A24IST&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=Childhood%20bone%20marrow%20monosomy%207%20syndrome:%20A%20familial%20disorder?&rft.jtitle=The%20Journal%20of%20pediatrics&rft.au=Carroll,%20William%20L.&rft.date=1985-10&rft.volume=107&rft.issue=4&rft.spage=578&rft.epage=580&rft.pages=578-580&rft.issn=0022-3476&rft.eissn=1097-6833&rft.coden=JOPDAB&rft_id=info:doi/10.1016/S0022-3476(85)80027-5&rft_dat=%3Cproquest_cross%3E76394968%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=76394968&rft_id=info:pmid/3862804&rft_els_id=S0022347685800275&rfr_iscdi=true