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A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32

Overview of attention for article published in BMC Medical Genomics, November 2010
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Title
A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32
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

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%