Saeidian, A. H., Vahidnezhad, H., Youssefian, L., Sotudeh, S., Sargazi, M., Zeinali, S., & Uitto, J. (2019). Hypotrichosis with juvenile macular dystrophy: Combination of whole‐genome sequencing and genome‐wide homozygosity mapping identifies a large deletion in CDH3 initially undetected by whole‐exome sequencing—A lesson from next‐generation sequencing. Mol Genet Genomic Med.
Chicago-стиль цитированияSaeidian, Amir Hossein, Hassan Vahidnezhad, Leila Youssefian, Soheila Sotudeh, Meisam Sargazi, Sirous Zeinali, and Jouni Uitto. "Hypotrichosis With Juvenile Macular Dystrophy: Combination of Whole‐genome Sequencing and Genome‐wide Homozygosity Mapping Identifies a Large Deletion in CDH3 Initially Undetected By Whole‐exome Sequencing—A Lesson From Next‐generation Sequencing." Mol Genet Genomic Med 2019.
MLA-цитированиеSaeidian, Amir Hossein, et al. "Hypotrichosis With Juvenile Macular Dystrophy: Combination of Whole‐genome Sequencing and Genome‐wide Homozygosity Mapping Identifies a Large Deletion in CDH3 Initially Undetected By Whole‐exome Sequencing—A Lesson From Next‐generation Sequencing." Mol Genet Genomic Med 2019.