Lundsgaard, M., Le, V. Q., Ernst, A., Laugaard-Jacobsen, H. C., Rasmussen, K., Pedersen, I. S., & Petersen, M. B. (2017). De novo KAT6B Mutation Identified with Whole-Exome Sequencing in a Girl with Say-Barber/Biesecker/Young-Simpson Syndrome. Mol Syndromol.
Citación estilo ChicagoLundsgaard, Malene, Vang Q. Le, Anja Ernst, Hans C. Laugaard-Jacobsen, Kirsten Rasmussen, Inge S. Pedersen, y Michael B. Petersen. "De Novo KAT6B Mutation Identified With Whole-Exome Sequencing in a Girl With Say-Barber/Biesecker/Young-Simpson Syndrome." Mol Syndromol 2017.
Cita MLALundsgaard, Malene, et al. "De Novo KAT6B Mutation Identified With Whole-Exome Sequencing in a Girl With Say-Barber/Biesecker/Young-Simpson Syndrome." Mol Syndromol 2017.
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