 |
 |
Search
- Page Path
-
- HOME
- Search
- Comparison of the copy-neutral loss of heterozygosity identified from whole-exome sequencing data using three different tools
-
Gang-Taik Lee
, Yeun-Jun Chung - Genomics Inform. 2022;20(1):e4. Published online March 31, 2022
-
Full text 
PubReader 
ePub 
PDF 
Supplementary Material
- Whole-exome sequencing analysis in a case of primary congenital glaucoma due to the partial uniparental isodisomy
-
Parisima Ghaffarian Zavarzadeh
, Morteza Bonyadi, Zahra Abedi - Genomics Inform. 2022;20(3):e28. Published online September 30, 2022
-
Full text PubReader ePub PDF
- Two novel mutations in ALDH18A1 and SPG11 gene found by whole-exome sequencing in spastic paraplegia disease patients in Iran
-
Sajad Rafiee Komachali, Zakieh Siahpoosh, Mansoor Salehi
- Genomics Inform. 2022;20(3):e30. Published online September 30, 2022
-
Full text PubReader ePub PDF
- Somatic Mutations from Whole Exome Sequencing Analysis of the Patients with Biliary Tract Cancer
-
Kyong-Ah Yoon, Sang Myung Woo, Yun-Hee Kim, Sun-Young Kong, Sung-Sik Han, Sang-Jae Park, Woo Jin Lee
- Genomics Inform. 2018;16(4):e35. Published online December 28, 2018
-
Full text PubReader ePub PDF Supplementary Material
- ARTICLE CATEGORY
- Editorial Office
-
Room No. 806, 193 Mallijae-ro, Jung-gu, Seoul 04501, Korea
Tel: +82-2-558-9394 Fax: +82-2-558-9434 E-mail: kogo3@kogo.or.kr
Copyright © 2025 by Korea Genome Organization.
