Genetic Confirmation of Congenital Factor V Deficiency in Korean Patients

por Park, Chang-Hun, Yoo, Kiyoung, Lee, Ki-O, Kim, Sun-Hee, Sung, Ki-Woong, Kim, Hee-Jin
Publicado 2016

Sequence variation data of F8 and F9 genes in functionally validated control individuals: implications on the molecular diagnosis of hemophilia

por Seo, Ja Young, Jang, Mi-Ae, Kim, Hee-Jung, Lee, Ki-O, Kim, Sun-Hee, Kim, Hee-Jin
Publicado 2013

Congenital factor V deficiency from compound heterozygous mutations with a novel variant c.2426del (p.Pro809Hisfs(∗)2) in the F5 gene: A case report

por Park, Chang-Hun, Park, Min-Seung, Lee, Ki-O, Kim, Sun-Hee, Park, Young Shil, Kim, Hee-Jin
Publicado 2020

Poor Prognostic Implication of ASXL1 Mutations in Korean Patients With Chronic Myelomonocytic Leukemia

por Kim, Hyun-Young, Lee, Ki-O, Park, Silvia, Jang, Jun Ho, Jung, Chul Won, Kim, Sun-Hee, Kim, Hee-Jin
Publicado 2018

Next‐generation sequencing reveals unique combination of mutations in cis of CSF3R in atypical chronic myeloid leukemia

por Yun, Jae Won, Yoon, Jung, Jung, Chul Won, Lee, Ki‐O, Kim, Jong Won, Kim, Sun‐Hee, Kim, Hee‐Jin
Publicado 2019

Molecular Genetics of von Willebrand Disease in Korean Patients: Novel Variants and Limited Diagnostic Utility of Multiplex Ligation-Dependent Probe Amplification Analyses

por Kim, Hee-Jung, Kim, Soon Ki, Yoo, Ki-Young, Lee, Ki-O, Yun, Jae Won, Kim, Sun-Hee, Kim, Hee-Jin, Park, Sang Kyu
Publicado 2019

Sequence Variations and Haplotypes of the GJB2 Gene Revealed by Resequencing of 192 Chromosomes from the General Population in Korea

por Kim, Hee-Jung, Park, Chang-Hun, Kim, Hee-Jin, Lee, Ki-O, Won, Hong-Hee, Ko, Moon-Hee, Chu, Hosuk, Cho, Yang-Sun, Chung, Won-Ho, Kim, Jong-Won, Hong, Sung Hwa
Publicado 2010