Artigo Acesso aberto Revisado por pares

Spondylocarpotarsal synostosis: Long‐term follow‐up of a case due to FLNB mutations

2008; Wiley; Volume: 146A; Issue: 9 Linguagem: Inglês

10.1002/ajmg.a.32303

ISSN

1552-4833

Autores

Nicola Brunetti‐Pierri, Valentina Esposito, Daniele De Brasi, Dario Maria Mattiacci, Deborah Krakow, Brendan Lee, Mariacarolina Salerno,

Tópico(s)

Child Abuse and Related Trauma

Resumo

American Journal of Medical Genetics Part AVolume 146A, Issue 9 p. 1230-1233 Research Letter Spondylocarpotarsal synostosis: Long-term follow-up of a case due to FLNB mutations† Nicola Brunetti-Pierri, Corresponding Author Nicola Brunetti-Pierri [email protected] Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, TexasDepartment of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, T607, Houston, TX 77030.Search for more papers by this authorValentina Esposito, Valentina Esposito Department of Pediatrics, Federico II University of Naples, Naples, ItalySearch for more papers by this authorDaniele De Brasi, Daniele De Brasi Department of Pediatrics, Federico II University of Naples, Naples, ItalySearch for more papers by this authorDario Maria Mattiacci, Dario Maria Mattiacci Department of Pediatrics, Federico II University of Naples, Naples, ItalySearch for more papers by this authorDeborah Krakow, Deborah Krakow Medical Genetics Institute, Cedars-Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, CaliforniaSearch for more papers by this authorBrendan Lee, Brendan Lee Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, Texas Howard Hughes Medical Institute, Houston, TexasSearch for more papers by this authorMariacarolina Salerno, Mariacarolina Salerno Department of Pediatrics, Federico II University of Naples, Naples, ItalySearch for more papers by this author Nicola Brunetti-Pierri, Corresponding Author Nicola Brunetti-Pierri [email protected] Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, TexasDepartment of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, T607, Houston, TX 77030.Search for more papers by this authorValentina Esposito, Valentina Esposito Department of Pediatrics, Federico II University of Naples, Naples, ItalySearch for more papers by this authorDaniele De Brasi, Daniele De Brasi Department of Pediatrics, Federico II University of Naples, Naples, ItalySearch for more papers by this authorDario Maria Mattiacci, Dario Maria Mattiacci Department of Pediatrics, Federico II University of Naples, Naples, ItalySearch for more papers by this authorDeborah Krakow, Deborah Krakow Medical Genetics Institute, Cedars-Sinai Medical Center, David Geffen School of Medicine at UCLA, Los Angeles, CaliforniaSearch for more papers by this authorBrendan Lee, Brendan Lee Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, Texas Howard Hughes Medical Institute, Houston, TexasSearch for more papers by this authorMariacarolina Salerno, Mariacarolina Salerno Department of Pediatrics, Federico II University of Naples, Naples, ItalySearch for more papers by this author First published: 03 April 2008 https://doi.org/10.1002/ajmg.a.32303Citations: 6 † How to cite this article: Brunetti-Pierri N, Esposito V, De Brasi D, Mattiacci DM, Krakow D, Lee B, Salerno M. 2008. Spondylocarpotarsal synostosis: Long-term follow-up of a case due to FLNB mutations. Am J Med Genet Part A 146A:1230–1233. 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 Citing Literature Volume146A, Issue91 May 2008Pages 1230-1233 RelatedInformation

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