Baschal, E. E., Wethey, C. I., Swindle, K., Baschal, R. M., Gowan, K., Tang, N. L., . . . Miller, N. H. (2014). Exome Sequencing Identifies a Rare HSPG2 Variant Associated with Familial Idiopathic Scoliosis. Genetics Society of America.
Chicago Style CitationBaschal, Erin E., et al. Exome Sequencing Identifies a Rare HSPG2 Variant Associated With Familial Idiopathic Scoliosis. Genetics Society of America, 2014.
MLA CitationBaschal, Erin E., et al. Exome Sequencing Identifies a Rare HSPG2 Variant Associated With Familial Idiopathic Scoliosis. Genetics Society of America, 2014.
Warning: These citations may not always be 100% accurate.