Duvdevani, M. P., Pettersson, M., Eisfeldt, J., Avraham, O., Dagan, J., Frumkin, A., . . . Harel, T. (2020). Whole genome sequencing reveals complex chromosome rearrangement disrupting NIPBL in infant with Cornelia de Lange syndrome. Am J Med Genet A.

Duvdevani, Morasha Plesser, Maria Pettersson, Jesper Eisfeldt, Ortal Avraham, Judith Dagan, Ayala Frumkin, James R. Lupski, Anna Lindstrand, und Tamar Harel. "Whole Genome Sequencing Reveals Complex Chromosome Rearrangement Disrupting NIPBL in Infant With Cornelia De Lange Syndrome." Am J Med Genet A 2020.

Duvdevani, Morasha Plesser, et al. "Whole Genome Sequencing Reveals Complex Chromosome Rearrangement Disrupting NIPBL in Infant With Cornelia De Lange Syndrome." Am J Med Genet A 2020.