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6p22.3 deletion: report of a patient with autism, severe intellectual disability and electroencephalographic anomalies

Overview of attention for article published in Molecular Cytogenetics, January 2013
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Title
6p22.3 deletion: report of a patient with autism, severe intellectual disability and electroencephalographic anomalies
Published in
Molecular Cytogenetics, January 2013
DOI 10.1186/1755-8166-6-4
Pubmed ID
Authors

Daniela Di Benedetto, Giuseppa Di Vita, Corrado Romano, Mariangela Lo Giudice, Girolamo Aurelio Vitello, Marinella Zingale, Lucia Grillo, Lucia Castiglia, Sebastiano Antonino Musumeci, Marco Fichera

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 45 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Japan 1 2%
Italy 1 2%
Unknown 43 96%

Demographic breakdown

Readers by professional status Count As %
Researcher 11 24%
Student > Ph. D. Student 6 13%
Student > Master 6 13%
Other 4 9%
Professor > Associate Professor 4 9%
Other 8 18%
Unknown 6 13%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 9 20%
Medicine and Dentistry 9 20%
Agricultural and Biological Sciences 8 18%
Psychology 4 9%
Neuroscience 2 4%
Other 5 11%
Unknown 8 18%