APA (7th ed.) Citation

Racine, C., Garde, A., Martz, O., Safraou, H., Eluard, V., Rousseau, T., . . . Faivre, L. (2025). First Prenatal Case of Genotypically and Phenotypically Overlapping Double Molecular Diagnosis of Van den Ende–Gupta and 22q11.2 Deletion Syndromes. Molecular Genetics & Genomic Medicine, 13(4), 1. https://doi.org/10.1002/mgg3.70096

Chicago Style (17th ed.) Citation

Racine, Caroline, et al. "First Prenatal Case of Genotypically and Phenotypically Overlapping Double Molecular Diagnosis of Van Den Ende–Gupta and 22q11.2 Deletion Syndromes." Molecular Genetics & Genomic Medicine 13, no. 4 (2025): 1. https://doi.org/10.1002/mgg3.70096.

MLA (9th ed.) Citation

Racine, Caroline, et al. "First Prenatal Case of Genotypically and Phenotypically Overlapping Double Molecular Diagnosis of Van Den Ende–Gupta and 22q11.2 Deletion Syndromes." Molecular Genetics & Genomic Medicine, vol. 13, no. 4, 2025, p. 1, https://doi.org/10.1002/mgg3.70096.