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Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype

Overview of attention for article published in Orphanet Journal of Rare Diseases, December 2011
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Title
Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype
Published in
Orphanet Journal of Rare Diseases, December 2011
DOI 10.1186/1750-1172-6-88
Pubmed ID
Authors

Swinnen FK, Coucke PJ, De Paepe AM, Symoens S, Malfait F, Gentile FV, Sangiorgi L, D'Eufemia P, Celli M, Garretsen TJ, Cremers CW, Dhooge IJ, De Leenheer EM, Freya KR Swinnen, Paul J Coucke, Anne M De Paepe, Sofie Symoens, Fransiska Malfait, Filomena V Gentile, Luca Sangiorgi, Patrizia D'Eufemia, Mauro Celli, Ton JTM Garretsen, Cor WRJ Cremers, Ingeborg JM Dhooge, Els MR De Leenheer

Mendeley readers

The data shown below were compiled from readership statistics for 32 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Turkey 1 3%
Unknown 31 97%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 16%
Student > Doctoral Student 5 16%
Other 4 13%
Student > Bachelor 3 9%
Student > Master 3 9%
Other 11 34%
Unknown 1 3%
Readers by discipline Count As %
Medicine and Dentistry 13 41%
Agricultural and Biological Sciences 5 16%
Nursing and Health Professions 3 9%
Biochemistry, Genetics and Molecular Biology 3 9%
Engineering 2 6%
Other 4 13%
Unknown 2 6%