Hannah, W. B., DeBrosse, S., Kinghorn, B., Strausbaugh, S., Aitken, M. L., Rosenfeld, M., . . . Zariwala, M. A. (2019). The expanding phenotype of OFD1‐related disorders: Hemizygous loss‐of‐function variants in three patients with primary ciliary dyskinesia. Mol Genet Genomic Med.
Chicago Style citaatHannah, William B., Suzanne DeBrosse, BreAnna Kinghorn, Steven Strausbaugh, Moira L. Aitken, Margaret Rosenfeld, Whitney E. Wolf, Michael R. Knowles, en Maimoona A. Zariwala. "The Expanding Phenotype of OFD1‐related Disorders: Hemizygous Loss‐of‐function Variants in Three Patients With Primary Ciliary Dyskinesia." Mol Genet Genomic Med 2019.
MLA citatieHannah, William B., et al. "The Expanding Phenotype of OFD1‐related Disorders: Hemizygous Loss‐of‐function Variants in Three Patients With Primary Ciliary Dyskinesia." Mol Genet Genomic Med 2019.