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.
Citação norma ChicagoSaeidian, 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.
Deismireacht MLASaeidian, 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.