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Expanding the phenotype of craniofrontonasal syndrome: two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia

Overview of attention for article published in European Journal of Human Genetics, April 2006
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22 Mendeley
Title
Expanding the phenotype of craniofrontonasal syndrome: two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia
Published in
European Journal of Human Genetics, April 2006
DOI 10.1038/sj.ejhg.5201633
Pubmed ID
Authors

Pradeep C Vasudevan, Stephen R F Twigg, John B Mulliken, Jackie A Cook, Oliver W J Quarrell, Andrew O M Wilkie

Mendeley readers

The data shown below were compiled from readership statistics for 22 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Belgium 1 5%
Unknown 21 95%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 23%
Student > Master 4 18%
Professor 3 14%
Student > Ph. D. Student 3 14%
Student > Postgraduate 2 9%
Other 5 23%
Readers by discipline Count As %
Medicine and Dentistry 8 36%
Agricultural and Biological Sciences 6 27%
Biochemistry, Genetics and Molecular Biology 4 18%
Unspecified 3 14%
Psychology 1 5%
Other 0 0%