Deismireacht APA

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 Chicago

Saeidian, 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 MLA

Saeidian, 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.

Rabhadh: D'fhéadfadh nach mbeadh na deismireachtaí seo 100% cruinn i gcónaí.