Spectrum of Mutations in Noonan Syndrome and Their Correlation with PhenotypesBeom Hee Lee, Han‐Wook Yoo, Jae‐Min Kim et al.|The Journal of Pediatrics|2011Cited by 96
Diagnostic yield of targeted gene panel sequencing to identify the genetic etiology of disorders of sex developmentJa Hye Kim, Jin‐Ho Choi, Eungu Kang et al.|Molecular and Cellular Endocrinology|2017Cited by 78
A review of the literature on common CYP17A1 mutations in adults with 17-hydroxylase/17,20-lyase deficiency, a case series of such mutations among Koreans and functional characteristics of a novel mutationYoo‐Mi Kim, Han‐Wook Yoo, Min‐Ji Kang et al.|Metabolism|2013Cited by 76
Clinical and Functional Characteristics of a Novel Heterozygous Mutation of the<i>IGF1R</i>Gene and IGF1R Haploinsufficiency due to Terminal 15q26.2->qter Deletion in Patients with Intrauterine Growth Retardation and Postnatal Catch-Up Growth FailureJin‐Ho Choi, Han‐Wook Yoo, Eul‐Ju Seo et al.|The Journal of Clinical Endocrinology & Metabolism|2010Cited by 63
High Frequency of <b><i>DUOX2</i></b> Mutations in Transient or Permanent Congenital Hypothyroidism with Eutopic Thyroid GlandsHye Young Jin, Han‐Wook Yoo, Sun‐Hee Heo et al.|Hormone Research in Paediatrics|2014Cited by 60