APA (7th ed.) Citation

Favier, M., Delanne, J., Gorincour, G., Faivre, L., Racine, C., Philippe, C., . . . Mau‐Them, F. T. (2024). Early prenatal diagnosis of causative homozygous variants in ASCC1 in a fetus with cystic hygroma and additional homozygous variants of unknown significance associated with a neurological phenotype not visible in early gestation: Dual diagnosis or not? Prenatal diagnosis, 44(3), 352-356. https://doi.org/10.1002/pd.6519

Chicago Style (17th ed.) Citation

Favier, Maud, et al. "Early Prenatal Diagnosis of Causative Homozygous Variants in ASCC1 in a Fetus with Cystic Hygroma and Additional Homozygous Variants of Unknown Significance Associated with a Neurological Phenotype Not Visible in Early Gestation: Dual Diagnosis or Not?" Prenatal Diagnosis 44, no. 3 (2024): 352-356. https://doi.org/10.1002/pd.6519.

MLA (9th ed.) Citation

Favier, Maud, et al. "Early Prenatal Diagnosis of Causative Homozygous Variants in ASCC1 in a Fetus with Cystic Hygroma and Additional Homozygous Variants of Unknown Significance Associated with a Neurological Phenotype Not Visible in Early Gestation: Dual Diagnosis or Not?" Prenatal Diagnosis, vol. 44, no. 3, 2024, pp. 352-356, https://doi.org/10.1002/pd.6519.