Childhood bone marrow monosomy 7 syndrome: A familial disorder?
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Veröffentlicht in: | The Journal of pediatrics 1985-10, Vol.107 (4), p.578-580 |
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container_issue | 4 |
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container_title | The Journal of pediatrics |
container_volume | 107 |
creator | Carroll, William L. Morgan, Rodman Glader, Bertil E. |
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doi_str_mv | 10.1016/S0022-3476(85)80027-5 |
format | Article |
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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. 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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> |
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ispartof | The Journal of pediatrics, 1985-10, Vol.107 (4), p.578-580 |
issn | 0022-3476 1097-6833 |
language | eng |
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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? |
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