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SNP genotyping to screen for a common deletion in CHARGE Syndrome

Overview of attention for article published in BMC Medical Genomics, February 2005
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Title
SNP genotyping to screen for a common deletion in CHARGE Syndrome
Published in
BMC Medical Genomics, February 2005
DOI 10.1186/1471-2350-6-8
Pubmed ID
Authors

Seema R Lalani, Arsalan M Safiullah, Susan D Fernbach, Michael Phillips, Carlos A Bacino, Laura M Molinari, Nancy L Glass, Jeffrey A Towbin, William J Craigen, John W Belmont

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 %
Italy 1 6%
Brazil 1 6%
Unknown 16 89%

Demographic breakdown

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