MEA, S., HE, V., & AM, B. (2023). A novel mutation in PTHLH in a family with a variable phenotype with brachydactyly, short stature, oligodontia and developmental delay. Bone reports, 19, 101699. https://doi.org/10.1016/j.bonr.2023.101699
Chicago Style (17th ed.) CitationMEA, Scheffer-Rath, Veenstra-Knol HE, and Boot AM. "A Novel Mutation in PTHLH in a Family with a Variable Phenotype with Brachydactyly, Short Stature, Oligodontia and Developmental Delay." Bone Reports 19 (2023): 101699. https://doi.org/10.1016/j.bonr.2023.101699.
MLA (9th ed.) CitationMEA, Scheffer-Rath, et al. "A Novel Mutation in PTHLH in a Family with a Variable Phenotype with Brachydactyly, Short Stature, Oligodontia and Developmental Delay." Bone Reports, vol. 19, 2023, p. 101699, https://doi.org/10.1016/j.bonr.2023.101699.