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 | ||
---|---|---|---|---|---|
15,472 | Dovepress* | 14,283+ | 1,802 | 16,085 | |
PubMed Central* | 1,189 | 263 | 1,452 | ||
Totals | 15,472 | 2,065 | 17,537 | ||
*Since 23 March 2018 |
View citations on PubMed Central and Google Scholar