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Papers published by Dr William Lopez-Quintero:
Corrigendum
Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype [Corrigendum]
Pachajoa H, López-Quintero W, Vanegas S, Montoya CL, Ramírez-Montaño D
The Application of Clinical Genetics 2018, 11:75-76
Published Date: 31 May 2018
Case report
Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype
Pachajoa H, López-Quintero W, Vanegas S, Montoya CL, Ramírez-Montaño D
The Application of Clinical Genetics 2018, 11:15-21
Published Date: 23 March 2018