Cost-effective BRCA Testing in Advanced Ovarian Cancer

por Kim, Myungshin
Publicado 2023

Extranasal natural killer/T-cell lymphoma initially presenting as myelofibrosis

por Jang, Woori, Kim, Myungshin
Publicado 2016

Current insights into inherited bone marrow failure syndromes

por Chung, Nack-Gyun, Kim, Myungshin
Publicado 2014

Diagnostic approaches for inherited hemolytic anemia in the genetic era

por Kim, Yonggoo, Park, Joonhong, Kim, Myungshin
Publicado 2017

Comparison of In Silico Tools for Splice-Altering Variant Prediction Using Established Spliceogenic Variants: An End-User's Point of View

por Jang, Woori, Park, Joonhong, Chae, Hyojin, Kim, Myungshin
Publicado 2022

Exon sequencing of the alpha-2-globin gene for the differential diagnosis of central cyanosis in newborns: a case report

por Shin, Chungwoo, Hong, Mee, Kim, Myungshin, Lee, Jung Hyun
Publicado 2019

Sex Chromosomes Are Severely Disrupted in Gastric Cancer Cell Lines

por Oh, Sooeun, Min, Kyoungmi, Kim, Myungshin, Lee, Suk Kyeong
Publicado 2020

Phenotype of a Patient With a 1p36.11-p35.3 Interstitial Deletion Encompassing the AHDC1

por Park, Hae-Yeon, Kim, Myungshin, Jang, Woori, Jang, Dae-Hyun
Publicado 2017

Clinical Significance of Composition and Functional Diversity of the Vaginal Microbiome in Recurrent Vaginitis

por Kim, Min Jeong, Lee, Seungok, Kwon, Mi Yeon, Kim, Myungshin
Publicado 2022

A Novel HNPP Phenotype in Charcot-Marie-Tooth Type 2E With c.1319C>T Missense Mutation in the NEFL Gene

por Choi, Ko-Eun, Yim, Jisook, Kim, Myungshin, Lee, Jung Hwan
Publicado 2022

White blood cell differential counts in severely leukopenic samples: a comparative analysis of different solutions available in modern laboratory hematology

por Kim, Ah Hyun, Lee, Wonbae, Kim, Myungshin, Kim, Yonggoo, Han, Kyungja
Publicado 2014

Molecular Features of Three Children Diagnosed With Early T-Cell Precursor Acute Lymphoblastic Leukemia

por Park, Dongjin, Kim, Myungshin, Kim, Yonggoo, Han, Kyungja, Lee, Jae Wook
Publicado 2016

Molecular analysis of the PAX6 gene for congenital aniridia in the Korean population: Identification of four novel mutations

por Park, Shin Hae, Kim, Man Soo, Chae, Hyojin, Kim, Yonggoo, Kim, Myungshin
Publicado 2012

X-Linked Spondyloepiphyseal Dysplasia Tarda: Identification of a TRAPPC2 Mutation in a Korean Pedigree

por Ryu, Hyejin, Park, Joonhong, Chae, Hyojin, Kim, Myungshin, Kim, Yonggoo, Ok, In-Young
Publicado 2012

Patient With Delayed Development Resulting From De Novo Duplication of 7q36.1-q36.3 and Deletion of 9p24.3

por Choi, Asayeon, Oh, Ja-Young, Kim, Myungshin, Jang, Woori, Jang, Dae-Hyun
Publicado 2017

Transient Neonatal Diabetes Mellitus in SHORT Syndrome: A Case Report

por Kim, Shin-Hee, Kim, Minsung, Yim, Jisook, Kim, Myungshin, Jang, Dae-Hyun
Publicado 2021

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

por Yim, Jisook, Kim, Kyoung Bo, Kim, Minsun, Lee, Gun Dong, Kim, Myungshin
Publicado 2022

Renal hypouricemia as the cause of exercise-induced acute kidney injury

por Lee, Haeun, Kang, Donghyuk, Lee, Hanbi, Yim, Jisook, Kim, Myungshin, Park, Cheol Whee
Publicado 2023

T618I-Mutated Colony Stimulating Factor 3 Receptor in Chronic Neutrophilic Leukemia and Chronic Myelomonocytic Leukemia Patients who Underwent Allogeneic Stem Cell Transplantation

por Lee, Sung-Eun, Jo, Irene, Jang, Woori, Kim, Yonggoo, Han, Kyungja, Kim, Myungshin
Publicado 2015

Comparison of Targeted Next-Generation and Sanger Sequencing for the BRCA1 and BRCA2 Mutation Screening

por Park, Joonhong, Jang, Woori, Chae, Hyojin, Kim, Yonggoo, Chi, Hyun Young, Kim, Myungshin
Publicado 2016