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Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome

Overview of attention for article published in BMC Medical Genomics, February 2011
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Citations

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45 Mendeley
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Title
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome
Published in
BMC Medical Genomics, February 2011
DOI 10.1186/1471-2350-12-21
Pubmed ID
Authors

Saima Riazuddin, Zubair M Ahmed, Rashmi S Hegde, Shaheen N Khan, Idrees Nasir, Uzma Shaukat, Sheikh Riazuddin, John A Butman, Andrew J Griffith, Thomas B Friedman, Byung Yoon Choi

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 %
United States 2 4%
Unknown 43 96%

Demographic breakdown

Readers by professional status Count As %
Student > Postgraduate 8 18%
Other 5 11%
Student > Master 5 11%
Student > Ph. D. Student 4 9%
Student > Bachelor 3 7%
Other 8 18%
Unknown 12 27%
Readers by discipline Count As %
Medicine and Dentistry 14 31%
Agricultural and Biological Sciences 6 13%
Biochemistry, Genetics and Molecular Biology 5 11%
Computer Science 1 2%
Psychology 1 2%
Other 4 9%
Unknown 14 31%