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, Se-Min Lee 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, Yoo‐Mi Kim et al.|Hormone Research in Paediatrics|2014Cited by 60