You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output.
Click here to find out more.
Mendeley readers
Title |
Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case report
|
---|---|
Published in |
BMC Medical Genomics, November 2014
|
DOI | 10.1186/s12881-014-0125-2 |
Pubmed ID | |
Authors |
Shiyu Luo, Wen Huang, Qiuping Xia, Yan Xia, Qian Du, Lingqian Wu, Ranhui Duan |
Mendeley readers
The data shown below were compiled from readership statistics for 19 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 19 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Researcher | 5 | 26% |
Student > Bachelor | 3 | 16% |
Student > Master | 3 | 16% |
Student > Doctoral Student | 2 | 11% |
Student > Ph. D. Student | 1 | 5% |
Other | 3 | 16% |
Unknown | 2 | 11% |
Readers by discipline | Count | As % |
---|---|---|
Biochemistry, Genetics and Molecular Biology | 5 | 26% |
Medicine and Dentistry | 4 | 21% |
Psychology | 3 | 16% |
Agricultural and Biological Sciences | 2 | 11% |
Nursing and Health Professions | 2 | 11% |
Other | 1 | 5% |
Unknown | 2 | 11% |