Dyfyniad APA

Lao, Q., Mallappa, A., Rueda Faucz, F., Joyal, E., Veeraraghavan, P., Chen, W., & Merke, D. P. (2020). A TNXB splice donor site variant as a cause of hypermobility type Ehlers–Danlos syndrome in patients with congenital adrenal hyperplasia. Mol Genet Genomic Med.

Dyfyniad Arddull Chicago

Lao, Qizong, Ashwini Mallappa, Fabio Rueda Faucz, Elizabeth Joyal, Padmasree Veeraraghavan, Wuyan Chen, and Deborah P. Merke. "A TNXB Splice Donor Site Variant As a Cause of Hypermobility Type Ehlers–Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia." Mol Genet Genomic Med 2020.

Dyfyniad MLA

Lao, Qizong, et al. "A TNXB Splice Donor Site Variant As a Cause of Hypermobility Type Ehlers–Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia." Mol Genet Genomic Med 2020.

Rhybudd: Mae'n bosib nad yw'r dyfyniadau hyn bob amser yn 100% cywir.