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Molecular characterization of two novel intronic variants of NIPBL gene detected in unrelated Cornelia de Lange syndrome patients

Overview of attention for article published in BMC Medical Genomics, January 2019
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18 Mendeley
Title
Molecular characterization of two novel intronic variants of NIPBL gene detected in unrelated Cornelia de Lange syndrome patients
Published in
BMC Medical Genomics, January 2019
DOI 10.1186/s12881-018-0738-y
Pubmed ID
Authors

Natalia Krawczynska, Jolanta Wierzba, Jacek Jasiecki, Bartosz Wasag

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 18 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 18 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 22%
Researcher 3 17%
Student > Bachelor 2 11%
Student > Master 2 11%
Lecturer 1 6%
Other 1 6%
Unknown 5 28%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 5 28%
Medicine and Dentistry 4 22%
Agricultural and Biological Sciences 1 6%
Immunology and Microbiology 1 6%
Neuroscience 1 6%
Other 0 0%
Unknown 6 33%