Ok-Hwa Kim

A Single Recurrent Mutation in the 5′-UTR of IFITM5 Causes Osteogenesis Imperfecta Type V

Tae‐Joon Cho, Kyung-Eun Lee, Sook-Kyung Lee et al. · The American Journal of Human Genetics · 2012 · 257 citations · Full text

Single Recurrent Mutation, Developmental Biology, Bone Morphogenic Protein +5

Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia

Su Jin Kim, Tadeusz Biegański, Young Bae Sohn et al. · Human Genetics · 2011 · 83 citations

Developmental Anomaly, Developmental Biology, Mendelian Disorder +8

Comparison of Clinico-Radiological Features between Congenital Cystic Neuroblastoma and Neonatal Adrenal Hemorrhagic Pseudocyst

Hong Eo, Ji Hye Kim, Kyung Mi Jang et al. · Korean Journal of Radiology · 2011 · 43 citations · Full text

Identification and<i>In Vivo</i>Functional Characterization of Novel Compound Heterozygous<i>BMP1</i>Variants in Osteogenesis Imperfecta

Sung Yoon Cho, P. V. Asharani, Ok-Hwa Kim et al. · Human Mutation · 2014 · 30 citations

Developmental Anomaly, Radial Head, Developmental Biology +14

Novel COL9A3 mutation in a family diagnosed with multiple epiphyseal dysplasia: a case report

Changhoon Jeong, Jae Young Lee, Ji‐Yeon Kim et al. · BMC Musculoskeletal Disorders · 2014 · 25 citations · Full text