Cite

Identification of a novel TGFBR1 mutation in a Loeys–Dietz syndrome type II patient with vascular Ehlers–Danlos syndrome phenotype.

MLA

Drera, B., et al. “Identification of a Novel TGFBR1 Mutation in a Loeys–Dietz Syndrome Type II Patient with Vascular Ehlers–Danlos Syndrome Phenotype.” Clinical Genetics, vol. 73, no. 3, Mar. 2008, pp. 290–93. EBSCOhost, https://doi.org/10.1111/j.1399-0004.2007.00942.x.



APA

Drera, B., Tadini, G., Barlati, S., & Colombi, M. (2008). Identification of a novel TGFBR1 mutation in a Loeys–Dietz syndrome type II patient with vascular Ehlers–Danlos syndrome phenotype. Clinical Genetics, 73(3), 290–293. https://doi.org/10.1111/j.1399-0004.2007.00942.x



Chicago

Drera, B., G. Tadini, S. Barlati, and M. Colombi. 2008. “Identification of a Novel TGFBR1 Mutation in a Loeys–Dietz Syndrome Type II Patient with Vascular Ehlers–Danlos Syndrome Phenotype.” Clinical Genetics 73 (3): 290–93. doi:10.1111/j.1399-0004.2007.00942.x.