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Mendeley readers
| Title |
A case report of T-box 1 mutation causing phenotypic features of chromosome 22q11.2 deletion syndrome
|
|---|---|
| Published in |
Clinical Diabetes and Endocrinology, August 2019
|
| DOI | 10.1186/s40842-019-0087-6 |
| Pubmed ID | |
| Authors |
Raad A. Haddad, Gregory A. Clines, Jennifer A. Wyckoff |
Mendeley readers
The data shown below were compiled from readership statistics for 20 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Unknown | 20 | 100% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Student > Ph. D. Student | 3 | 15% |
| Other | 2 | 10% |
| Student > Doctoral Student | 2 | 10% |
| Researcher | 2 | 10% |
| Student > Master | 2 | 10% |
| Other | 2 | 10% |
| Unknown | 7 | 35% |
| Readers by discipline | Count | As % |
|---|---|---|
| Biochemistry, Genetics and Molecular Biology | 3 | 15% |
| Medicine and Dentistry | 3 | 15% |
| Unspecified | 1 | 5% |
| Linguistics | 1 | 5% |
| Agricultural and Biological Sciences | 1 | 5% |
| Other | 3 | 15% |
| Unknown | 8 | 40% |