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Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients

Overview of attention for article published in Molecular Cytogenetics, April 2015
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38 Mendeley
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Title
Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients
Published in
Molecular Cytogenetics, April 2015
DOI 10.1186/s13039-015-0130-y
Pubmed ID
Authors

Nancy Choucair, Joelle Abou Ghoch, Sandra Corbani, Pierre Cacciagli, Cecile Mignon-Ravix, Nabiha Salem, Nadine Jalkh, Sandra El Sabbagh, Ali Fawaz, Tony Ibrahim, Laurent Villard, André Mégarbané, Eliane Chouery

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 38 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 38 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 7 18%
Student > Master 6 16%
Student > Bachelor 6 16%
Student > Doctoral Student 4 11%
Other 3 8%
Other 9 24%
Unknown 3 8%
Readers by discipline Count As %
Medicine and Dentistry 12 32%
Biochemistry, Genetics and Molecular Biology 7 18%
Agricultural and Biological Sciences 5 13%
Psychology 4 11%
Nursing and Health Professions 3 8%
Other 3 8%
Unknown 4 11%