Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil
BACKGROUND Nonsyndromic cleft lip with or without cleft palate is a relatively common craniofacial defect with multifactorial inheritance. The association of the rs987525 single nucleotide variant, located in a gene desert at 8q24.21 region, has been consistently replicated in European populations....
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Veröffentlicht in: | Birth defects research. A Clinical and molecular teratology 2012-06, Vol.94 (6), p.464-468 |
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creator | Brito, Luciano Abreu Paranaiba, Lívia Máris Ribeiro Bassi, Camila Fernandes Silva Masotti, Cibele Malcher, Carolina Schlesinger, David Rocha, Katia Maria Cruz, Lucas Alvizi Bárbara, Lígia Kobayashi Alonso, Nivaldo Franco, Diogo Bagordakis, Elizabete Martelli Jr, Hercílio Meyer, Diogo Coletta, Ricardo D. Passos-Bueno, Maria Rita |
description | BACKGROUND
Nonsyndromic cleft lip with or without cleft palate is a relatively common craniofacial defect with multifactorial inheritance. The association of the rs987525 single nucleotide variant, located in a gene desert at 8q24.21 region, has been consistently replicated in European populations. We performed a structured association approach combined with transcriptional analysis of the MYC gene to dissect the role of rs987525 in oral clefting susceptibility in the ethnically admixed Brazilian population.
METHODS
We performed the association study conditioned on the individual ancestry proportions in a sample of 563 patients and 336 controls, and in an independent sample of 221 patients and 261 controls. The correlation between rs987525 genotypes and MYC transcriptional levels in orbicularis oris muscle mesenchymal stem cells was also investigated in 42 patients and 4 controls.
RESULTS
We found a significant association in the larger sample (p = 0.0016; OR = 1.80 [95% confidence interval {CI}, 1.21–2.69], for heterozygous genotype, and 2.71 [95% CI, 1.47–4.96] for homozygous genotype). We did not find a significant correlation between rs987525 genotypes and MYC transcriptional levels (p = 0.14; r = −0.22, Spearman Correlation).
CONCLUSIONS
We present a positive association of rs987525 in the Brazilian population for the first time, and it is likely that the European contribution to our population is driving this association. We also cannot discard a role of rs987515 in MYC regulation, because this locus behaves as an expression quantitative locus of MYC in another tissue. Birth Defects Research (Part A), 2012. © 2012 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/bdra.23011 |
format | Article |
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Nonsyndromic cleft lip with or without cleft palate is a relatively common craniofacial defect with multifactorial inheritance. The association of the rs987525 single nucleotide variant, located in a gene desert at 8q24.21 region, has been consistently replicated in European populations. We performed a structured association approach combined with transcriptional analysis of the MYC gene to dissect the role of rs987525 in oral clefting susceptibility in the ethnically admixed Brazilian population.
METHODS
We performed the association study conditioned on the individual ancestry proportions in a sample of 563 patients and 336 controls, and in an independent sample of 221 patients and 261 controls. The correlation between rs987525 genotypes and MYC transcriptional levels in orbicularis oris muscle mesenchymal stem cells was also investigated in 42 patients and 4 controls.
RESULTS
We found a significant association in the larger sample (p = 0.0016; OR = 1.80 [95% confidence interval {CI}, 1.21–2.69], for heterozygous genotype, and 2.71 [95% CI, 1.47–4.96] for homozygous genotype). We did not find a significant correlation between rs987525 genotypes and MYC transcriptional levels (p = 0.14; r = −0.22, Spearman Correlation).
CONCLUSIONS
We present a positive association of rs987525 in the Brazilian population for the first time, and it is likely that the European contribution to our population is driving this association. We also cannot discard a role of rs987515 in MYC regulation, because this locus behaves as an expression quantitative locus of MYC in another tissue. Birth Defects Research (Part A), 2012. © 2012 Wiley Periodicals, Inc.</description><identifier>ISSN: 1542-0752</identifier><identifier>EISSN: 1542-0760</identifier><identifier>DOI: 10.1002/bdra.23011</identifier><identifier>PMID: 22511506</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>8q24 gene desert ; Brazil - epidemiology ; Case-Control Studies ; Chromosomes, Human, Pair 8 ; cleft lip ; Cleft Lip - ethnology ; Cleft Lip - genetics ; cleft palate ; Cleft Palate - ethnology ; Cleft Palate - genetics ; common disease-common variant ; Continental Population Groups ; Female ; Genetic Loci ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; heritability ; Heterozygote ; Homozygote ; Humans ; Male ; mesenchymal stem cells ; MYC transcriptional levels ; Polymorphism, Single Nucleotide ; Proto-Oncogene Proteins c-myc - genetics ; rs1476165 ; rs2099897 ; rs987525 ; Transcription, Genetic</subject><ispartof>Birth defects research. A Clinical and molecular teratology, 2012-06, Vol.94 (6), p.464-468</ispartof><rights>Copyright © 2012 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3671-a7701ca356d6048b6e89603717cc8970bfe1acd6d8fd85d6649416d997718f273</citedby><cites>FETCH-LOGICAL-c3671-a7701ca356d6048b6e89603717cc8970bfe1acd6d8fd85d6649416d997718f273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbdra.23011$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbdra.23011$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22511506$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brito, Luciano Abreu</creatorcontrib><creatorcontrib>Paranaiba, Lívia Máris Ribeiro</creatorcontrib><creatorcontrib>Bassi, Camila Fernandes Silva</creatorcontrib><creatorcontrib>Masotti, Cibele</creatorcontrib><creatorcontrib>Malcher, Carolina</creatorcontrib><creatorcontrib>Schlesinger, David</creatorcontrib><creatorcontrib>Rocha, Katia Maria</creatorcontrib><creatorcontrib>Cruz, Lucas Alvizi</creatorcontrib><creatorcontrib>Bárbara, Lígia Kobayashi</creatorcontrib><creatorcontrib>Alonso, Nivaldo</creatorcontrib><creatorcontrib>Franco, Diogo</creatorcontrib><creatorcontrib>Bagordakis, Elizabete</creatorcontrib><creatorcontrib>Martelli Jr, Hercílio</creatorcontrib><creatorcontrib>Meyer, Diogo</creatorcontrib><creatorcontrib>Coletta, Ricardo D.</creatorcontrib><creatorcontrib>Passos-Bueno, Maria Rita</creatorcontrib><title>Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil</title><title>Birth defects research. A Clinical and molecular teratology</title><addtitle>Birth Defects Research Part A: Clinical and Molecular Teratology</addtitle><description>BACKGROUND
Nonsyndromic cleft lip with or without cleft palate is a relatively common craniofacial defect with multifactorial inheritance. The association of the rs987525 single nucleotide variant, located in a gene desert at 8q24.21 region, has been consistently replicated in European populations. We performed a structured association approach combined with transcriptional analysis of the MYC gene to dissect the role of rs987525 in oral clefting susceptibility in the ethnically admixed Brazilian population.
METHODS
We performed the association study conditioned on the individual ancestry proportions in a sample of 563 patients and 336 controls, and in an independent sample of 221 patients and 261 controls. The correlation between rs987525 genotypes and MYC transcriptional levels in orbicularis oris muscle mesenchymal stem cells was also investigated in 42 patients and 4 controls.
RESULTS
We found a significant association in the larger sample (p = 0.0016; OR = 1.80 [95% confidence interval {CI}, 1.21–2.69], for heterozygous genotype, and 2.71 [95% CI, 1.47–4.96] for homozygous genotype). We did not find a significant correlation between rs987525 genotypes and MYC transcriptional levels (p = 0.14; r = −0.22, Spearman Correlation).
CONCLUSIONS
We present a positive association of rs987525 in the Brazilian population for the first time, and it is likely that the European contribution to our population is driving this association. We also cannot discard a role of rs987515 in MYC regulation, because this locus behaves as an expression quantitative locus of MYC in another tissue. Birth Defects Research (Part A), 2012. © 2012 Wiley Periodicals, Inc.</description><subject>8q24 gene desert</subject><subject>Brazil - epidemiology</subject><subject>Case-Control Studies</subject><subject>Chromosomes, Human, Pair 8</subject><subject>cleft lip</subject><subject>Cleft Lip - ethnology</subject><subject>Cleft Lip - genetics</subject><subject>cleft palate</subject><subject>Cleft Palate - ethnology</subject><subject>Cleft Palate - genetics</subject><subject>common disease-common variant</subject><subject>Continental Population Groups</subject><subject>Female</subject><subject>Genetic Loci</subject><subject>Genetic Predisposition to Disease</subject><subject>Genome-Wide Association Study</subject><subject>heritability</subject><subject>Heterozygote</subject><subject>Homozygote</subject><subject>Humans</subject><subject>Male</subject><subject>mesenchymal stem cells</subject><subject>MYC transcriptional levels</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Proto-Oncogene Proteins c-myc - genetics</subject><subject>rs1476165</subject><subject>rs2099897</subject><subject>rs987525</subject><subject>Transcription, Genetic</subject><issn>1542-0752</issn><issn>1542-0760</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFLwzAYhoMoOqcXf4DkKEJnkrZJe3RTp1gmDEXwEtIkHdGs2ZIWnb_ezs0dvXzfd3jel48HgDOMBhghclUqLwYkRhjvgR5OExIhRtH-7k7JETgO4b1jY8bYITgiJMU4RbQHJlM9M66G2ZIk0AQoYGiD1IvGlMaaZgWtk22AlfOwdnVY1cq7uZHQeWGhtLpqTD2DpoZDL76NPQEHlbBBn253H7zc3T6P7qPiafwwui4iGVOGI8EYwlLEKVUUJVlJdZZTFDPMpMxyhspKYyEVVVmlslRRmuQJpirPGcNZRVjcBxeb3oV3y1aHhs9N97a1otauDRwjglDajTV6uUGldyF4XfGFN3PhVx3E1_742h__9dfB59vetpxrtUP_hHUA3gCfxurVP1V8eDO9_iuNNhkTGv21ywj_wSmLWcpfJ2NeFNO3SUExf4x_ABp3iDU</recordid><startdate>201206</startdate><enddate>201206</enddate><creator>Brito, Luciano Abreu</creator><creator>Paranaiba, Lívia Máris Ribeiro</creator><creator>Bassi, Camila Fernandes Silva</creator><creator>Masotti, Cibele</creator><creator>Malcher, Carolina</creator><creator>Schlesinger, David</creator><creator>Rocha, Katia Maria</creator><creator>Cruz, Lucas Alvizi</creator><creator>Bárbara, Lígia Kobayashi</creator><creator>Alonso, Nivaldo</creator><creator>Franco, Diogo</creator><creator>Bagordakis, Elizabete</creator><creator>Martelli Jr, Hercílio</creator><creator>Meyer, Diogo</creator><creator>Coletta, Ricardo D.</creator><creator>Passos-Bueno, Maria Rita</creator><general>Wiley Subscription Services, Inc., A Wiley Company</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>201206</creationdate><title>Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil</title><author>Brito, Luciano Abreu ; Paranaiba, Lívia Máris Ribeiro ; Bassi, Camila Fernandes Silva ; Masotti, Cibele ; Malcher, Carolina ; Schlesinger, David ; Rocha, Katia Maria ; Cruz, Lucas Alvizi ; Bárbara, Lígia Kobayashi ; Alonso, Nivaldo ; Franco, Diogo ; Bagordakis, Elizabete ; Martelli Jr, Hercílio ; Meyer, Diogo ; Coletta, Ricardo D. ; Passos-Bueno, Maria Rita</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3671-a7701ca356d6048b6e89603717cc8970bfe1acd6d8fd85d6649416d997718f273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>8q24 gene desert</topic><topic>Brazil - epidemiology</topic><topic>Case-Control Studies</topic><topic>Chromosomes, Human, Pair 8</topic><topic>cleft lip</topic><topic>Cleft Lip - ethnology</topic><topic>Cleft Lip - genetics</topic><topic>cleft palate</topic><topic>Cleft Palate - ethnology</topic><topic>Cleft Palate - genetics</topic><topic>common disease-common variant</topic><topic>Continental Population Groups</topic><topic>Female</topic><topic>Genetic Loci</topic><topic>Genetic Predisposition to Disease</topic><topic>Genome-Wide Association Study</topic><topic>heritability</topic><topic>Heterozygote</topic><topic>Homozygote</topic><topic>Humans</topic><topic>Male</topic><topic>mesenchymal stem cells</topic><topic>MYC transcriptional levels</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Proto-Oncogene Proteins c-myc - genetics</topic><topic>rs1476165</topic><topic>rs2099897</topic><topic>rs987525</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brito, Luciano Abreu</creatorcontrib><creatorcontrib>Paranaiba, Lívia Máris Ribeiro</creatorcontrib><creatorcontrib>Bassi, Camila Fernandes Silva</creatorcontrib><creatorcontrib>Masotti, Cibele</creatorcontrib><creatorcontrib>Malcher, Carolina</creatorcontrib><creatorcontrib>Schlesinger, David</creatorcontrib><creatorcontrib>Rocha, Katia Maria</creatorcontrib><creatorcontrib>Cruz, Lucas Alvizi</creatorcontrib><creatorcontrib>Bárbara, Lígia Kobayashi</creatorcontrib><creatorcontrib>Alonso, Nivaldo</creatorcontrib><creatorcontrib>Franco, Diogo</creatorcontrib><creatorcontrib>Bagordakis, Elizabete</creatorcontrib><creatorcontrib>Martelli Jr, Hercílio</creatorcontrib><creatorcontrib>Meyer, Diogo</creatorcontrib><creatorcontrib>Coletta, Ricardo D.</creatorcontrib><creatorcontrib>Passos-Bueno, Maria Rita</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>Birth defects research. A Clinical and molecular teratology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brito, Luciano Abreu</au><au>Paranaiba, Lívia Máris Ribeiro</au><au>Bassi, Camila Fernandes Silva</au><au>Masotti, Cibele</au><au>Malcher, Carolina</au><au>Schlesinger, David</au><au>Rocha, Katia Maria</au><au>Cruz, Lucas Alvizi</au><au>Bárbara, Lígia Kobayashi</au><au>Alonso, Nivaldo</au><au>Franco, Diogo</au><au>Bagordakis, Elizabete</au><au>Martelli Jr, Hercílio</au><au>Meyer, Diogo</au><au>Coletta, Ricardo D.</au><au>Passos-Bueno, Maria Rita</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil</atitle><jtitle>Birth defects research. A Clinical and molecular teratology</jtitle><addtitle>Birth Defects Research Part A: Clinical and Molecular Teratology</addtitle><date>2012-06</date><risdate>2012</risdate><volume>94</volume><issue>6</issue><spage>464</spage><epage>468</epage><pages>464-468</pages><issn>1542-0752</issn><eissn>1542-0760</eissn><abstract>BACKGROUND
Nonsyndromic cleft lip with or without cleft palate is a relatively common craniofacial defect with multifactorial inheritance. The association of the rs987525 single nucleotide variant, located in a gene desert at 8q24.21 region, has been consistently replicated in European populations. We performed a structured association approach combined with transcriptional analysis of the MYC gene to dissect the role of rs987525 in oral clefting susceptibility in the ethnically admixed Brazilian population.
METHODS
We performed the association study conditioned on the individual ancestry proportions in a sample of 563 patients and 336 controls, and in an independent sample of 221 patients and 261 controls. The correlation between rs987525 genotypes and MYC transcriptional levels in orbicularis oris muscle mesenchymal stem cells was also investigated in 42 patients and 4 controls.
RESULTS
We found a significant association in the larger sample (p = 0.0016; OR = 1.80 [95% confidence interval {CI}, 1.21–2.69], for heterozygous genotype, and 2.71 [95% CI, 1.47–4.96] for homozygous genotype). We did not find a significant correlation between rs987525 genotypes and MYC transcriptional levels (p = 0.14; r = −0.22, Spearman Correlation).
CONCLUSIONS
We present a positive association of rs987525 in the Brazilian population for the first time, and it is likely that the European contribution to our population is driving this association. We also cannot discard a role of rs987515 in MYC regulation, because this locus behaves as an expression quantitative locus of MYC in another tissue. Birth Defects Research (Part A), 2012. © 2012 Wiley Periodicals, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>22511506</pmid><doi>10.1002/bdra.23011</doi><tpages>5</tpages></addata></record> |
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subjects | 8q24 gene desert Brazil - epidemiology Case-Control Studies Chromosomes, Human, Pair 8 cleft lip Cleft Lip - ethnology Cleft Lip - genetics cleft palate Cleft Palate - ethnology Cleft Palate - genetics common disease-common variant Continental Population Groups Female Genetic Loci Genetic Predisposition to Disease Genome-Wide Association Study heritability Heterozygote Homozygote Humans Male mesenchymal stem cells MYC transcriptional levels Polymorphism, Single Nucleotide Proto-Oncogene Proteins c-myc - genetics rs1476165 rs2099897 rs987525 Transcription, Genetic |
title | Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil |
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