Leone, M. P., Palumbo, P., Palumbo, O., Di Muro, E., Chetta, M., Laforgia, N., . . . Bukvic, N. (2020). The recurrent SETBP1 c.2608G > A, p.(Gly870Ser) variant in a patient with Schinzel-Giedion syndrome: An illustrative case of the utility of whole exome sequencing in a critically ill neonate. Ital J Pediatr.
Stile di citazione ChicagoLeone, Maria Pia, et al. "The Recurrent SETBP1 C.2608G > A, P.(Gly870Ser) Variant in a Patient With Schinzel-Giedion Syndrome: An Illustrative Case of the Utility of Whole Exome Sequencing in a Critically Ill Neonate." Ital J Pediatr 2020.
Citazione MLALeone, Maria Pia, et al. "The Recurrent SETBP1 C.2608G > A, P.(Gly870Ser) Variant in a Patient With Schinzel-Giedion Syndrome: An Illustrative Case of the Utility of Whole Exome Sequencing in a Critically Ill Neonate." Ital J Pediatr 2020.