APA (7th ed.) Citation

SH, E., WE, S., MM, A., A, E., SM, S., AE, E., . . . EM, A. (2025). Fetal Phenotyping and Whole Exome Sequencing for 12 Egyptian Families With Serine Biosynthesis Defect: Novel Clinical and Allelic Findings With a Founder Effect. Prenatal diagnosis, 45(2), 204. https://doi.org/10.1002/pd.6697

Chicago Style (17th ed.) Citation

SH, El-Dessouky, et al. "Fetal Phenotyping and Whole Exome Sequencing for 12 Egyptian Families With Serine Biosynthesis Defect: Novel Clinical and Allelic Findings With a Founder Effect." Prenatal Diagnosis 45, no. 2 (2025): 204. https://doi.org/10.1002/pd.6697.

MLA (9th ed.) Citation

SH, El-Dessouky, et al. "Fetal Phenotyping and Whole Exome Sequencing for 12 Egyptian Families With Serine Biosynthesis Defect: Novel Clinical and Allelic Findings With a Founder Effect." Prenatal Diagnosis, vol. 45, no. 2, 2025, p. 204, https://doi.org/10.1002/pd.6697.