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SOD-A and chromosome 21. Conflicting findings in a familial translocation (9p24;21q214)
A balanced maternal chromosome translocation (9p24;21q214) resulted in two offspring with unbalanced karyotypes. One of these, a girl trisomic for both segment 9pter to 9p24 and segment 21pter to 21q214, was found to have a SOD-A activity not significantly different from those found in a group of fi...
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Published in: | Human genetics 1981-01, Vol.57 (2), p.220-223 |
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container_issue | 2 |
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container_title | Human genetics |
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creator | Leschot, N J Slater, R M Joenje, H Becker-Bloemkolk, M J de Nef, J J |
description | A balanced maternal chromosome translocation (9p24;21q214) resulted in two offspring with unbalanced karyotypes. One of these, a girl trisomic for both segment 9pter to 9p24 and segment 21pter to 21q214, was found to have a SOD-A activity not significantly different from those found in a group of five cases with trisomy 21. However, clinical evaluation of this girl revealed no symptoms of the Down syndrome. These findings suggest that, providing the gene dosage theory is correct, the gene for SOD-A is probably localized on chromosome 21 proximal to, or in, band q21. |
doi_str_mv | 10.1007/BF00282029 |
format | article |
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These findings suggest that, providing the gene dosage theory is correct, the gene for SOD-A is probably localized on chromosome 21 proximal to, or in, band q21.</description><identifier>ISSN: 0340-6717</identifier><identifier>EISSN: 1432-1203</identifier><identifier>DOI: 10.1007/BF00282029</identifier><identifier>PMID: 7228038</identifier><language>eng</language><publisher>Germany</publisher><subject>Child ; Chromosome Aberrations - enzymology ; Chromosome Aberrations - genetics ; Chromosome Disorders ; Chromosomes, Human, 21-22 and Y ; Chromosomes, Human, 6-12 and X ; Female ; Humans ; Infant, Newborn ; Intellectual Disability - genetics ; Karyotyping ; Male ; Superoxide Dismutase - genetics ; Translocation, Genetic</subject><ispartof>Human genetics, 1981-01, Vol.57 (2), p.220-223</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7228038$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Leschot, N J</creatorcontrib><creatorcontrib>Slater, R M</creatorcontrib><creatorcontrib>Joenje, H</creatorcontrib><creatorcontrib>Becker-Bloemkolk, M J</creatorcontrib><creatorcontrib>de Nef, J J</creatorcontrib><title>SOD-A and chromosome 21. Conflicting findings in a familial translocation (9p24;21q214)</title><title>Human genetics</title><addtitle>Hum Genet</addtitle><description>A balanced maternal chromosome translocation (9p24;21q214) resulted in two offspring with unbalanced karyotypes. One of these, a girl trisomic for both segment 9pter to 9p24 and segment 21pter to 21q214, was found to have a SOD-A activity not significantly different from those found in a group of five cases with trisomy 21. However, clinical evaluation of this girl revealed no symptoms of the Down syndrome. These findings suggest that, providing the gene dosage theory is correct, the gene for SOD-A is probably localized on chromosome 21 proximal to, or in, band q21.</description><subject>Child</subject><subject>Chromosome Aberrations - enzymology</subject><subject>Chromosome Aberrations - genetics</subject><subject>Chromosome Disorders</subject><subject>Chromosomes, Human, 21-22 and Y</subject><subject>Chromosomes, Human, 6-12 and X</subject><subject>Female</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Intellectual Disability - genetics</subject><subject>Karyotyping</subject><subject>Male</subject><subject>Superoxide Dismutase - genetics</subject><subject>Translocation, Genetic</subject><issn>0340-6717</issn><issn>1432-1203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><recordid>eNpFkEtLw0AURgdRaq1u3AuzEhVS752ZPAZXtT6h0IWKy3AzyehIkmkz6cJ_b6RFV2dz-Pg4jJ0iTBEgvb59ABCZAKH32BiVFBEKkPtsDFJBlKSYHrKjEL4AMNYiHrFRKkQGMhuz95flXTTj1JbcfHa-8cE3FRc45XPf2tqZ3rUf3Lq2HBi4azlxS42rHdW876gNtTfUO9_yC70S6kbgWqC6PGYHlupQnew4YW8P96_zp2ixfHyezxaREQr7iJKiAlUQUlrIONGkCwOGEkXJcF1ba7WmrEyUsaRUjKJQphBoM5NCGWMqJ-x8u7vq_HpThT5vXDBVXVNb-U3I0ziRMcQ4iFdb0XQ-hK6y-apzDXXfOUL-WzH_rzjIZ7vVTdFU5Z-6yyZ_AO4HaZg</recordid><startdate>19810101</startdate><enddate>19810101</enddate><creator>Leschot, N J</creator><creator>Slater, R M</creator><creator>Joenje, H</creator><creator>Becker-Bloemkolk, M J</creator><creator>de Nef, J J</creator><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>19810101</creationdate><title>SOD-A and chromosome 21. 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Conflicting findings in a familial translocation (9p24;21q214)</atitle><jtitle>Human genetics</jtitle><addtitle>Hum Genet</addtitle><date>1981-01-01</date><risdate>1981</risdate><volume>57</volume><issue>2</issue><spage>220</spage><epage>223</epage><pages>220-223</pages><issn>0340-6717</issn><eissn>1432-1203</eissn><abstract>A balanced maternal chromosome translocation (9p24;21q214) resulted in two offspring with unbalanced karyotypes. One of these, a girl trisomic for both segment 9pter to 9p24 and segment 21pter to 21q214, was found to have a SOD-A activity not significantly different from those found in a group of five cases with trisomy 21. However, clinical evaluation of this girl revealed no symptoms of the Down syndrome. These findings suggest that, providing the gene dosage theory is correct, the gene for SOD-A is probably localized on chromosome 21 proximal to, or in, band q21.</abstract><cop>Germany</cop><pmid>7228038</pmid><doi>10.1007/BF00282029</doi><tpages>4</tpages></addata></record> |
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source | Springer Online Journal Archives (Through 1996) |
subjects | Child Chromosome Aberrations - enzymology Chromosome Aberrations - genetics Chromosome Disorders Chromosomes, Human, 21-22 and Y Chromosomes, Human, 6-12 and X Female Humans Infant, Newborn Intellectual Disability - genetics Karyotyping Male Superoxide Dismutase - genetics Translocation, Genetic |
title | SOD-A and chromosome 21. Conflicting findings in a familial translocation (9p24;21q214) |
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