Hypertrophic cardiomyopathy in a girl with Cornelia de Lange syndrome due to mutation in SMC1A

Giuseppe Limongelli, Silvia Russo, Maria Cristina Digilio, Maura Masciadri, Giuseppe Pacileo, Fiorella Fratta, Francesca Martone, Valeria Maddaloni, Raffaella D'Alessandro, Paolo Calabro, Maria Giovanna Russo, Raffaele Calabro, Lidia Larizza

Research output: Contribution to journal › Article

Original languageEnglish
Pages (from-to)2127-2129
Number of pages3
JournalAmerican Journal of Medical Genetics, Part A
Volume152
Issue number8
DOIs
Publication statusPublished - Aug 2010

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Hypertrophic cardiomyopathy in a girl with Cornelia de Lange syndrome due to mutation in SMC1A. / Limongelli, Giuseppe; Russo, Silvia; Digilio, Maria Cristina; Masciadri, Maura; Pacileo, Giuseppe; Fratta, Fiorella; Martone, Francesca; Maddaloni, Valeria; D'Alessandro, Raffaella; Calabro, Paolo; Russo, Maria Giovanna; Calabro, Raffaele; Larizza, Lidia.

In: American Journal of Medical Genetics, Part A, Vol. 152, No. 8, 08.2010, p. 2127-2129.

Research output: Contribution to journal › Article

Limongelli, G, Russo, S, Digilio, MC, Masciadri, M, Pacileo, G, Fratta, F, Martone, F, Maddaloni, V, D'Alessandro, R, Calabro, P, Russo, MG, Calabro, R & Larizza, L 2010, 'Hypertrophic cardiomyopathy in a girl with Cornelia de Lange syndrome due to mutation in SMC1A', American Journal of Medical Genetics, Part A, vol. 152, no. 8, pp. 2127-2129. https://doi.org/10.1002/ajmg.a.33486
Limongelli G, Russo S, Digilio MC, Masciadri M, Pacileo G, Fratta F et al. Hypertrophic cardiomyopathy in a girl with Cornelia de Lange syndrome due to mutation in SMC1A. American Journal of Medical Genetics, Part A. 2010 Aug;152(8):2127-2129. https://doi.org/10.1002/ajmg.a.33486
Limongelli, Giuseppe ; Russo, Silvia ; Digilio, Maria Cristina ; Masciadri, Maura ; Pacileo, Giuseppe ; Fratta, Fiorella ; Martone, Francesca ; Maddaloni, Valeria ; D'Alessandro, Raffaella ; Calabro, Paolo ; Russo, Maria Giovanna ; Calabro, Raffaele ; Larizza, Lidia. / Hypertrophic cardiomyopathy in a girl with Cornelia de Lange syndrome due to mutation in SMC1A. In: American Journal of Medical Genetics, Part A. 2010 ; Vol. 152, No. 8. pp. 2127-2129.
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