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Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency

Overview of attention for article published in BMC Medical Genomics, November 2016
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Title
Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency
Published in
BMC Medical Genomics, November 2016
DOI 10.1186/s12881-016-0349-4
Pubmed ID
Authors

Birgitta Bergendal, Johanna Norderyd, Xiaolei Zhou, Joakim Klar, Niklas Dahl

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 55 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 55 100%

Demographic breakdown

Readers by professional status Count As %
Student > Postgraduate 7 13%
Student > Master 7 13%
Student > Ph. D. Student 6 11%
Unspecified 6 11%
Professor > Associate Professor 4 7%
Other 11 20%
Unknown 14 25%
Readers by discipline Count As %
Medicine and Dentistry 24 44%
Unspecified 6 11%
Biochemistry, Genetics and Molecular Biology 4 7%
Agricultural and Biological Sciences 4 7%
Nursing and Health Professions 1 2%
Other 2 4%
Unknown 14 25%