Myungshin Kim

发表

Clinical Features, Gene Alterations, and Outcomes in Prefibrotic and Overt Primary and Secondary Myelofibrotic Patients

B. Cho, Yoo-Jin Kim, Jae‐Ho Yoon, 2022, Cancers.

Cost-effective BRCA Testing in Advanced Ovarian Cancer

Myungshin Kim, 2022, Annals of laboratory medicine.

A case of Deletion of Chromosome 4p

Mi-Sook Lee, Sang-eun Lee, Seung-Cheol Lee, 2002 .

18p Deletion Syndrome Originating from Rare Unbalanced Whole-Arm Translocation between Chromosomes 13 and 18: A Case Report and Literature Review

J. Choi, Min Ho Jung, J. Yim, 2022, Children.

Adrenocortical carcinoma and a sporadic MEN1 mutation in a 3-year-old girl: a case report

Jae Wook Lee, W. Cho, Byung-Kyu Suh, 2022, Annals of pediatric endocrinology & metabolism.

Transient Neonatal Diabetes Mellitus in SHORT Syndrome: A Case Report

Myungshin Kim, D. Jang, S. Kim, 2021, Frontiers in Pediatrics.

Andersen–Tawil Syndrome With Novel Mutation in KCNJ2: Case Report

G. Lee, J. Yim, Myungshin Kim, 2022, Frontiers in Pediatrics.

A case of the novel mutation p.L311P in KRT5 causing localized epidermolysis bullosa simplex in East Asian population.

So Yeon Yun, Myungshin Kim, Young Min Park, 2023, Indian journal of dermatology, venereology and leprology.

Validation of Pathogenicity of Gene Variants in Fanconi Anemia Using Patient-derived Dermal Fibroblasts

Yonghwan Kim, N. Chung, Jung Bok Lee, 2022, Annals of Laboratory Medicine.

Multilevel Airway Stenosis Being Bypassed by a Customized Tracheostomy Tube in an Infant with Myhre Syndrome.

J. Ko, S. Kwon, Ji Hye Kim, 2021, Pediatric allergy, immunology, and pulmonology.

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

Jongsun Jung, O. Kim, Jiyeon Kim, 2014, BMC Musculoskeletal Disorders.