Article Versions Notes

Richter JE Jr., Samreen A, Vadlamudi C, Helmi H, Mohammad AN, Wierenga K, Hines S, Atwal PS, Caulfield TR. Genomic Observations of a Rare/Pathogenic SMAD3 Variant in Loeys–Dietz Syndrome 3 Confirmed by Protein Informatics and Structural Investigations. Medicina. 2019; 55(5):137. https://doi.org/10.3390/medicina55050137

Richter, John E., Jr., Ayesha Samreen, Charitha Vadlamudi, Haytham Helmi, Ahmed N. Mohammad, Klaas Wierenga, Stephanie Hines, Paldeep S. Atwal, and Thomas R. Caulfield. 2019. "Genomic Observations of a Rare/Pathogenic SMAD3 Variant in Loeys–Dietz Syndrome 3 Confirmed by Protein Informatics and Structural Investigations" Medicina 55, no. 5: 137. https://doi.org/10.3390/medicina55050137

Richter, J. E., Jr., Samreen, A., Vadlamudi, C., Helmi, H., Mohammad, A. N., Wierenga, K., Hines, S., Atwal, P. S., & Caulfield, T. R. (2019). Genomic Observations of a Rare/Pathogenic SMAD3 Variant in Loeys–Dietz Syndrome 3 Confirmed by Protein Informatics and Structural Investigations. Medicina, 55(5), 137. https://doi.org/10.3390/medicina55050137