SH, E., WE, S., MM, A., HA, M., MS, Z., R, M., . . . EM, A. (2025). Integrating Prenatal Exome Sequencing and Ultrasonographic Fetal Phenotyping for Assessment of Congenital Malformations: High Molecular Diagnostic Yield and Novel Phenotypic Expansions in a Consanguineous Cohort. Clinical genetics, 108(1), 33. https://doi.org/10.1111/cge.14712
Chicago Style (17th ed.) CitationSH, El-Dessouky, et al. "Integrating Prenatal Exome Sequencing and Ultrasonographic Fetal Phenotyping for Assessment of Congenital Malformations: High Molecular Diagnostic Yield and Novel Phenotypic Expansions in a Consanguineous Cohort." Clinical Genetics 108, no. 1 (2025): 33. https://doi.org/10.1111/cge.14712.
MLA (9th ed.) CitationSH, El-Dessouky, et al. "Integrating Prenatal Exome Sequencing and Ultrasonographic Fetal Phenotyping for Assessment of Congenital Malformations: High Molecular Diagnostic Yield and Novel Phenotypic Expansions in a Consanguineous Cohort." Clinical Genetics, vol. 108, no. 1, 2025, p. 33, https://doi.org/10.1111/cge.14712.
