APA (7th ed.) Citation

ER, W., LT, E., JA, R., S, K., LC, B., & DA, S. (2025). Recessive loss-of-function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine-Lubinsky syndrome. American journal of medical genetics. Part A, 197(1), e63845. https://doi.org/10.1002/ajmg.a.63845

Chicago Style (17th ed.) Citation

ER, Waskow, Emrick LT, Rosenfeld JA, Ketkar S, Burrage LC, and Scott DA. "Recessive Loss-of-function Variants in DPH1 Identified as the Molecular Cause in a Sibling Pair Previously Diagnosed with Fine-Lubinsky Syndrome." American Journal of Medical Genetics. Part A 197, no. 1 (2025): e63845. https://doi.org/10.1002/ajmg.a.63845.

MLA (9th ed.) Citation

ER, Waskow, et al. "Recessive Loss-of-function Variants in DPH1 Identified as the Molecular Cause in a Sibling Pair Previously Diagnosed with Fine-Lubinsky Syndrome." American Journal of Medical Genetics. Part A, vol. 197, no. 1, 2025, p. e63845, https://doi.org/10.1002/ajmg.a.63845.