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• W2067827684 abstract "American Journal of Medical Genetics Part AVolume 167, Issue 5 p. 1161-1164 Research Letter Recurrence of frontometaphyseal dysplasia in two sisters with a mutation in FLNA and an atypical paternal phenotype: Insights into genotype–phenotype correlation Debora Bertola, Corresponding Author Debora Bertola Faculdade de Medicina da Universidade de São Paulo, Unidade de Genética do Instituto da Criança, São Paulo, Brazil Correspondence to: Debora Bertola, Faculdade de Medicina da Universidade de São Paulo, Unidade de Genética do Instituto da Criança, Av. Dr. Enéas Carvalho de Aguiar, 647 São Paulo, São Paulo 05403.000, Brazil. E-mail: debora.bertola@usp.brSearch for more papers by this authorMaria Rita Passos-Bueno, Maria Rita Passos-Bueno University of São Paulo, Department of Biology, São Paulo, BrazilSearch for more papers by this authorAlexandre Pereira, Alexandre Pereira Instituto do Coração, Faculdade de Medicina da Universidade de Sâo Paulo, Cardiology, São Paulo, BrazilSearch for more papers by this authorChong Kim, Chong Kim Instituto da Criança, Pediatrics, São Paulo, BrazilSearch for more papers by this authorTim Morgan, Tim Morgan University of Otago, Dunedin School of Medicine, Department of Women's and Children's Health, New ZealandSearch for more papers by this authorStephen P. Robertson, Stephen P. Robertson University of Otago, Dunedin School of Medicine, Department of Women's and Children's Health, New ZealandSearch for more papers by this author Debora Bertola, Corresponding Author Debora Bertola Faculdade de Medicina da Universidade de São Paulo, Unidade de Genética do Instituto da Criança, São Paulo, Brazil Correspondence to: Debora Bertola, Faculdade de Medicina da Universidade de São Paulo, Unidade de Genética do Instituto da Criança, Av. Dr. Enéas Carvalho de Aguiar, 647 São Paulo, São Paulo 05403.000, Brazil. E-mail: debora.bertola@usp.brSearch for more papers by this authorMaria Rita Passos-Bueno, Maria Rita Passos-Bueno University of São Paulo, Department of Biology, São Paulo, BrazilSearch for more papers by this authorAlexandre Pereira, Alexandre Pereira Instituto do Coração, Faculdade de Medicina da Universidade de Sâo Paulo, Cardiology, São Paulo, BrazilSearch for more papers by this authorChong Kim, Chong Kim Instituto da Criança, Pediatrics, São Paulo, BrazilSearch for more papers by this authorTim Morgan, Tim Morgan University of Otago, Dunedin School of Medicine, Department of Women's and Children's Health, New ZealandSearch for more papers by this authorStephen P. Robertson, Stephen P. Robertson University of Otago, Dunedin School of Medicine, Department of Women's and Children's Health, New ZealandSearch for more papers by this author First published: 28 March 2015 https://doi.org/10.1002/ajmg.a.36981Citations: 2 Conflict of interest: None. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat Citing Literature Volume167, Issue5May 2015Pages 1161-1164 RelatedInformation" @default.
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• W2067827684 title "Recurrence of frontometaphyseal dysplasia in two sisters with a mutation in<i>FLNA</i>and an atypical paternal phenotype: Insights into genotype-phenotype correlation" @default.
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