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Mendeley readers
| Title |
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
|
|---|---|
| Published in |
BMC Medical Genomics, September 2011
|
| DOI | 10.1186/1471-2350-12-122 |
| Pubmed ID | |
| Authors |
Aimee L Fenwick, Sarah C Bowdin, Regan EM Klatt, Andrew OM Wilkie |
Mendeley readers
The data shown below were compiled from readership statistics for 21 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 21 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Student > Ph. D. Student | 4 | 19% |
| Student > Master | 4 | 19% |
| Professor | 3 | 14% |
| Student > Doctoral Student | 2 | 10% |
| Student > Bachelor | 2 | 10% |
| Other | 2 | 10% |
| Unknown | 4 | 19% |
| Readers by discipline | Count | As % |
|---|---|---|
| Biochemistry, Genetics and Molecular Biology | 7 | 33% |
| Agricultural and Biological Sciences | 6 | 29% |
| Medicine and Dentistry | 3 | 14% |
| Social Sciences | 1 | 5% |
| Sports and Recreations | 1 | 5% |
| Other | 0 | 0% |
| Unknown | 3 | 14% |