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, Beom Hee Lee et al.|The Journal of Clinical Endocrinology & Metabolism|2010Cited by 63