Dyfyniad APA

Hermanns, P., Khadouma, S., Shepherd, S., Mansor, M., Schulga, J., Jones, J., . . . Pohlenz, J. (2014). A novel mutation in the PAX8 promoter region causes permanent congenital hypothyroidism in a patient with Down’s Syndrome. Mol Cell Pediatr.

Dyfyniad Arddull Chicago

Hermanns, Pia, Sunia Khadouma, Scott Shepherd, Mohamed Mansor, John Schulga, J. Jones, M. Donaldson, and Joachim Pohlenz. "A Novel Mutation in the PAX8 Promoter Region Causes Permanent Congenital Hypothyroidism in a Patient With Down’s Syndrome." Mol Cell Pediatr 2014.

Dyfyniad MLA

Hermanns, Pia, et al. "A Novel Mutation in the PAX8 Promoter Region Causes Permanent Congenital Hypothyroidism in a Patient With Down’s Syndrome." Mol Cell Pediatr 2014.

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