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, 273.
https://doi.org/10.3390/genes14020273
AMA Style
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
Chicago/Turabian Style
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
APA Style
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
