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Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in FAM111A gene

Overview of attention for article published in International Journal of Pediatric Endocrinology, January 2017
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Citations

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28 Dimensions

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30 Mendeley
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Title
Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in FAM111A gene
Published in
International Journal of Pediatric Endocrinology, January 2017
DOI 10.1186/s13633-016-0041-7
Pubmed ID
Authors

Mary B. Abraham, Dong Li, Dave Tang, Susan M. O’Connell, Fiona McKenzie, Ee Mun Lim, Hakon Hakonarson, Michael A. Levine, Catherine S. Choong

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 30 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Brazil 1 3%
Unknown 29 97%

Demographic breakdown

Readers by professional status Count As %
Student > Master 4 13%
Student > Doctoral Student 3 10%
Student > Bachelor 3 10%
Student > Ph. D. Student 3 10%
Researcher 3 10%
Other 3 10%
Unknown 11 37%
Readers by discipline Count As %
Medicine and Dentistry 7 23%
Biochemistry, Genetics and Molecular Biology 6 20%
Nursing and Health Professions 1 3%
Pharmacology, Toxicology and Pharmaceutical Science 1 3%
Social Sciences 1 3%
Other 3 10%
Unknown 11 37%