Hypertrophic cardiomyopathy in a girl with Cornelia de Lange syndrome due to mutation in SMC1A
Copyright policy ) LIMONGELLI, Giuseppe; RUSSO S; DIGILIO MC; MASCIADRI M; PACILEO G; FRATTA F; MARTONE F; MADDALONI V; D'ALESSANDRO R; CALABRO', Paolo; RUSSO, Maria Giovanna; CALABRO', Raffaele; LARIZZA L.;
Hypertrophic cardiomyopathy in a girl with Cornelia de Lange syndrome due to mutation in SMC1A
Male, Cornelia de Lange syndrome ; SMC1A ; Hypertrophic Cardiomyopathy, Chromosomal Proteins, Non-Histone, Molecular Sequence Data, Mutation, Missense, Cell Cycle Proteins, Cardiomyopathy, Hypertrophic, Pedigree, De Lange Syndrome, Humans, Female, Amino Acid Sequence, Child, Structural Maintenance of Chromosome Protein 1
Male, Cornelia de Lange syndrome ; SMC1A ; Hypertrophic Cardiomyopathy, Chromosomal Proteins, Non-Histone, Molecular Sequence Data, Mutation, Missense, Cell Cycle Proteins, Cardiomyopathy, Hypertrophic, Pedigree, De Lange Syndrome, Humans, Female, Amino Acid Sequence, Child, Structural Maintenance of Chromosome Protein 1
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Citations provided by BIP!
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
Citations provided by BIP!popularityPopularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
Popularity provided by BIP! 25
Top 10%
Top 10%
Average
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