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Mendeley readers
Title |
A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32
|
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Published in |
BMC Medical Genomics, November 2010
|
DOI | 10.1186/1471-2350-11-165 |
Pubmed ID | |
Authors |
Kathryn Hattersley, Kate J Laurie, Jan E Liebelt, Jozef Gecz, Shane R Durkin, Jamie E Craig, Kathryn P Burdon |
Mendeley readers
The data shown below were compiled from readership statistics for 23 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
Country | Count | As % |
---|---|---|
Australia | 1 | 4% |
Unknown | 22 | 96% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Doctoral Student | 4 | 17% |
Researcher | 4 | 17% |
Other | 3 | 13% |
Student > Master | 3 | 13% |
Professor | 2 | 9% |
Other | 3 | 13% |
Unknown | 4 | 17% |
Readers by discipline | Count | As % |
---|---|---|
Psychology | 5 | 22% |
Agricultural and Biological Sciences | 4 | 17% |
Biochemistry, Genetics and Molecular Biology | 2 | 9% |
Medicine and Dentistry | 2 | 9% |
Nursing and Health Professions | 1 | 4% |
Other | 5 | 22% |
Unknown | 4 | 17% |