| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Systematic review of the clinical and genetic aspects of Prader-Willi syndrome. | Korean J Pediatr | 2011 | 0.78 |
| 2 | CYP21A2 mutation analysis in Korean patients with congenital adrenal hyperplasia using complementary methods: sequencing after long-range PCR and restriction fragment length polymorphism analysis with multiple ligation-dependent probe amplification assay. | Ann Lab Med | 2015 | 0.75 |