Bitar, T., Hleihel, W., Marouillat, S., Vonwill, S., Vuillaume, M., Soufia, M., . . . Andres, C. R. (2019). Identification of rare copy number variations reveals PJA2, APCS, SYNPO, and TAC1 as novel candidate genes in Autism Spectrum Disorders. Mol Genet Genomic Med.
Citação norma ChicagoBitar, Tania, Walid Hleihel, Sylviane Marouillat, Sandrine Vonwill, Marie‐Laure Vuillaume, Michel Soufia, Patrick Vourc'h, Frederic Laumonnier, and Christian R. Andres. "Identification of Rare Copy Number Variations Reveals PJA2, APCS, SYNPO, and TAC1 As Novel Candidate Genes in Autism Spectrum Disorders." Mol Genet Genomic Med 2019.
ציטוט MLABitar, Tania, et al. "Identification of Rare Copy Number Variations Reveals PJA2, APCS, SYNPO, and TAC1 As Novel Candidate Genes in Autism Spectrum Disorders." Mol Genet Genomic Med 2019.