Back to Journals » The Application of Clinical Genetics » Volume 11

Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype [Corrigendum]

Total article views   Abstract views HTML views PDF downloads Totals
2,314 Dovepress* 1,950 195+ 484 2,145
PubMed Central* 0 169 24 169
Totals 1,950 364 508 2,314
*Since 31 May 2018
+Since July 2016

View citations on PubMed Central and Google Scholar