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Mary L, Leclerc D, Labalme A, Bellaud P, Mazaud-Guittot S, Dréano S, Evrard B, Bigand A, Cauchoix A, Loget P, et al. Functional Assessment of a New PBX1 Variant in a 46,XY Fetus with Severe Syndromic Difference of Sexual Development through CRISPR-Cas9 Gene Editing. Genes. 2023; 14(2):273. https://doi.org/10.3390/genes14020273

Mary, Laura, Delphine Leclerc, Audrey Labalme, Pascale Bellaud, Séverine Mazaud-Guittot, Stéphane Dréano, Bertrand Evrard, Antoine Bigand, Aurélie Cauchoix, Philippe Loget, and et al. 2023. "Functional Assessment of a New PBX1 Variant in a 46,XY Fetus with Severe Syndromic Difference of Sexual Development through CRISPR-Cas9 Gene Editing" Genes 14, no. 2: 273. https://doi.org/10.3390/genes14020273

Mary, L., Leclerc, D., Labalme, A., Bellaud, P., Mazaud-Guittot, S., Dréano, S., Evrard, B., Bigand, A., Cauchoix, A., Loget, P., Lokchine, A., Cluzeau, L., Gilot, D., Belaud-Rotureau, M.-A., & Jaillard, S. (2023). Functional Assessment of a New PBX1 Variant in a 46,XY Fetus with Severe Syndromic Difference of Sexual Development through CRISPR-Cas9 Gene Editing. Genes, 14(2), 273. https://doi.org/10.3390/genes14020273