Myung S. Kim

Incheon St. Mary's Hospital
Seoul, Republic of Korea

Last Updated: 09/26/2026

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Found 12 publications

Isolated congenital vertebral anomaly and Sprengel's deformity in a WBP11 pathogenic variant.

Isolated congenital vertebral anomaly and Sprengel's deformity in a WBP11 pathogenic variant.

Journal: European journal of medical genetics

Published: July 03, 2024

The First Korean Child of Jalili Syndrome with a Novel Missense Mutation in Cation Transport Mediator 4 (CNNM4): A Case Report.

The First Korean Child of Jalili Syndrome with a Novel Missense Mutation in Cation Transport Mediator 4 (CNNM4): A Case Report.

Journal: Korean journal of ophthalmology : KJO

Published: November 03, 2022

Characteristics of amniotic mesenchymal stromal cells derived from term and preterm labor.

Characteristics of amniotic mesenchymal stromal cells derived from term and preterm labor.

Journal: Taiwanese journal of obstetrics & gynecology

Published: December 30, 2020

Maternal serum placental growth factor combined with second trimester aneuploidy screening to predict small-for-gestation neonates without preeclampsia.

Maternal serum placental growth factor combined with second trimester aneuploidy screening to predict small-for-gestation neonates without preeclampsia.

Journal: Taiwanese journal of obstetrics & gynecology

Published: August 20, 2017

Recurrent macrophage activation syndrome since toddler age in an adolescent boy with HLA B27 positive juvenile ankylosing spondylitis.

Recurrent macrophage activation syndrome since toddler age in an adolescent boy with HLA B27 positive juvenile ankylosing spondylitis.

Journal: Korean journal of pediatrics

Published: May 03, 2016

Mutational analysis of oncogenic CSF3R p.T618I in acute leukemias and common solid cancers.

Mutational analysis of oncogenic CSF3R p.T618I in acute leukemias and common solid cancers.

Journal: Annals of hematology

Published: October 30, 2014

Novel oncogenic PTPN11 mutations in myelodysplastic syndrome in Korean patients.

Novel oncogenic PTPN11 mutations in myelodysplastic syndrome in Korean patients.

Journal: Hematological oncology

Published: January 10, 2014

Perspectives on clinical informatics: integrating large-scale clinical, genomic, and health information for clinical care.

Perspectives on clinical informatics: integrating large-scale clinical, genomic, and health information for clinical care.

Journal: Genomics & informatics

Published: October 18, 2013

Somatic mutation of SPOP tumor suppressor gene is rare in breast, lung, liver cancers, and acute leukemias.

Somatic mutation of SPOP tumor suppressor gene is rare in breast, lung, liver cancers, and acute leukemias.

Journal: APMIS : acta pathologica, microbiologica, et immunologica Scandinavica

Published: December 12, 2012

Mutational analysis of splicing machinery genes SF3B1, U2AF1 and SRSF2 in myelodysplasia and other common tumors.

Mutational analysis of splicing machinery genes SF3B1, U2AF1 and SRSF2 in myelodysplasia and other common tumors.

Journal: International journal of cancer

Published: September 26, 2012

A case of familial X-linked thrombocytopenia with a novel WAS gene mutation.

A case of familial X-linked thrombocytopenia with a novel WAS gene mutation.

Journal: Korean journal of pediatrics

Published: August 17, 2012

Somatic mutation of IL7R exon 6 in acute leukemias and solid cancers.

Somatic mutation of IL7R exon 6 in acute leukemias and solid cancers.

Journal: Human pathology

Published: May 21, 2012

Showing 1-12 of 12

Last Updated: 09/26/2026