Claudia Montoya

All Stories

1. 
   Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype [Corrigendum]

   Article • The Application of Clinical Genetics, May 2018, Dove Medical Press

   Claudia Montoya, William López

2. 
   Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype

   Article • The Application of Clinical Genetics, March 2018, Dove Medical Press

   William López, Claudia Montoya