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Papers published by Dr Sara Vanegas:
Corrigendum
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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
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Achondrogenesis type 1A: clinical, histologic, molecular, and prenatal ultrasound diagnosis
Vanegas S, Sua LF, López-Tenorio J, Ramírez-Montaño D, Pachajoa H
The Application of Clinical Genetics 2018, 11:69-73
Published Date: 25 May 2018
Case report
![Highly-accessed](assets/img/article_icons/highly-accessed.png)
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