Hyon J Kim

发表

A Case of Fanconi Anemia Diagnosed by a Chromosome Breakage Test with Skin Fibroblasts

Kyung Bin Yun, S. Kim, Mee Jeong Lee, 2008 .

Acquisition of a BCR-ABL1 transcript in a patient with disease progression from MDS with fibrosis to AML with myelodysplasia-related changes.

Joon Seong Park, S. Jeong, J. Seok, 2011, Annals of clinical and laboratory science.

Phenotypic Analysis of Korean Patients with Abnormal Chromosomal Microarray in Patients with Unexplained Developmental Delay/Intellectual Disability

J. Lim, Hyo Jeong Kim, Hyon J Kim, 2018, Yonsei medical journal.

Acute Promyelocytic Leukemia With Complex Translocation t(5;17;15)(q35;q21;q22): Case Report and Review of the Literature

J. Choi, S. Cho, H. Jung, 2011, Journal of pediatric hematology/oncology.

A Korean family with KBG syndrome identified by ANKRD11 mutation, and phenotypic comparison of ANKRD11 mutation and 16q24.3 microdeletion.

W. Im, Hyon J Kim, Eunhae Cho, 2015, European journal of medical genetics.

Identifying the KAT6B Mutation via Diagnostic Exome Sequencing to Diagnose Say-Barber-Biesecker-Young-Simpson Syndrome in Three Generations of a Family

Y. Lee, Hyon J Kim, Yong Rok Kim, 2017, Annals of rehabilitation medicine.

[Two cases of acute myeloid leukemia with t(16;21)(p11;q22) and TLS/FUS-ERG fusion transcripts].

Joon Seong Park, S. Cho, Hyun Woo Lee, 2009, The Korean journal of laboratory medicine.

Acute myeloid leukemia with t(16;21)(q24;q22) and eosinophilia: case report and review of the literature.

W. Lee, S. Cho, H. Jung, 2010, Cancer genetics and cytogenetics.

A novel nonsense mutation of GPR143 gene in a Korean kindred with X-linked congenital nystagmus.

U. Kim, Hyon J Kim, Eunhae Cho, 2016, International journal of ophthalmology.