Hye Ran Lee

发表

A single recurrent mutation in the 5'-UTR of IFITM5 causes osteogenesis imperfecta type V.

In Ho Choi, Su Jeong Song, Daehyun Jeon, 2012, American journal of human genetics.

Distraction osteogenesis induces endothelial progenitor cell mobilization without inflammatory response in man.

In Ho Choi, Dong Yeon Lee, Moon Seok Park, 2010, Bone.

Pseudarthrosis of the Tibia Associated with Neurofibromatosis Type 1 Biologic Characteristics of Fibrous Hamartoma from Congenital

C. Chung, T. Cho, Joong-Bae Seo, 2009 .

Biologic characteristics of fibrous hamartoma from congenital pseudarthrosis of the tibia associated with neurofibromatosis type 1.

C. Chung, T. Cho, Joong-Bae Seo, 2008, The Journal of bone and joint surgery. American volume.

Mobilization of endothelial progenitor cells in fracture healing and distraction osteogenesis.

Dong Yeon Lee, C. Chung, T. Cho, 2008, Bone.

Novel missense loss-of-function mutations of WNT1 in an autosomal recessive Osteogenesis imperfecta patient.

T. Cho, Jong Hoon Park, Woo-Young Kim, 2017, European journal of medical genetics.

Autosomal Recessive Multiple Epiphyseal Dysplasia in a Korean Girl Caused by Novel Compound Heterozygous Mutations in the DTDST (SLC26A2) Gene

W. Park, Sung Im Cho, S. Park, 2010, Journal of Korean medical science.

Autosomal dominant brachyolmia: transient metaphyseal striations

T. Cho, O. Kim, K. Park, 2017, Skeletal Radiology.

Is double inactivation of the Nf1 gene responsible for the development of congenital pseudarthrosis of the tibia associated with NF1?

Dong Yeon Lee, C. Chung, M. Park, 2012, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

Disturbed Osteoblastic Differentiation of Fibrous Hamartoma Cell from Congenital Pseudarthrosis of the Tibia Associated with Neurofibromatosis Type I

Dong Yeon Lee, C. Chung, M. Park, 2011, Clinics in orthopedic surgery.

Enhancement of Vasculogenesis and Osteogenesis Using Granulocyte-Colony Stimulating Factor in the Rat Model of Tibial Distraction Osteogenesis

Dong Yeon Lee, T. Cho, S. Shin, 2011 .

Skeletal overgrowth syndrome caused by overexpression of C‐type natriuretic peptide in a girl with balanced chromosomal translocation, t(1;2)(q41;q37.1)

W. Park, S. Oh, J. Ko, 2015, American journal of medical genetics. Part A.

Extending the phenotype of BMPER-related skeletal dysplasias to ischiospinal dysostosis

T. Cho, G. Nishimura, E. Kuchinskaya, 2016, Orphanet Journal of Rare Diseases.

Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia.

O. Mäkitie, Dongsup Kim, G. Stewart, 2019, American journal of human genetics.

Wiedemann-Steiner Syndrome With 2 Novel KMT2A Mutations

Murim Choi, T. Cho, Jieun Seo, 2017, Journal of child neurology.

Physeal Growth Arrest by Excessive Compression: Histological, Biochemical, and Micro-CT Observations in Rabbits

T. Cho, J. Cheon, W. Yoo, 2011, Clinics in orthopedic surgery.

Wiedemann-Steiner Syndrome With 2 Novel KMT 2 A Mutations : Variable Severity in Psychomotor Development and Musculoskeletal Manifestation

Murim Choi, J. Ko, T. Cho, 2016 .

Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type.

Dongsup Kim, D. Kang, W. Park, 2011, American journal of human genetics.

Causes Osteogenesis Imperfecta Type V

Su Jeong Song, W. Park, Z. Lee, 2012 .

ACVR1 Gene Mutation in Sporadic Korean Patients with Fibrodysplasia Ossificans Progressiva

Dong Yeon Lee, C. Chung, M. Park, 2009, Journal of Korean medical science.