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 | ||
|---|---|---|---|---|---|
| 15,385 | Dovepress* | 14,196+ | 1,801 | 15,997 | |
| PubMed Central* | 1,189 | 263 | 1,452 | ||
| Totals | 15,385 | 2,064 | 17,449 | ||
| *Since 23 March 2018 | |||||
View citations on PubMed Central and Google Scholar