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.
Chicago Style CitationBitar, Tania, Walid Hleihel, Sylviane Marouillat, Sandrine Vonwill, Marie‐Laure Vuillaume, Michel Soufia, Patrick Vourc'h, Frederic Laumonnier, i 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.
Cita 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.