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Hypertrophic Cardiomyopathy in a Girl With Cornelia de Lange Syndrome Due to Mutation in SMC1A
Hypertrophic Cardiomyopathy in a Girl With Cornelia de Lange Syndrome Due to Mutation in SMC1A
2010
Giuseppe Limongelli
Silvia Russo
Maria Cristina Digilio
Maura Masciadri
Giuseppe Pacileo
Fiorella Fratta
Francesca Martone
Valeria Maddaloni
R. DAlessandro
Paolo Calabrò
Maria Giovanna Russo
Raffaele Calabrò
Lidia Larizza
Keywords:
SMC1A
Endocrinology
Cornelia de Lange Syndrome
Internal medicine
Mutation
Heart disease
Hypertrophic cardiomyopathy
Central nervous system disease
Girl
Biology
myocardial disease
Correction
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