Menu
Back to Journals » The Application of Clinical Genetics » Volume 11
Case report
Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype
| Total article views | HTML views | PDF downloads | Totals | ||
|---|---|---|---|---|---|
| 15,296 | Dovepress* | 14,110+ | 1,799 | 15,909 | |
| PubMed Central* | 1,186 | 261 | 1,447 | ||
| Totals | 15,296 | 2,060 | 17,356 | ||
| *Since 23 March 2018 | |||||
View citations on PubMed Central and Google Scholar