top of page
KOR
CONTACT
HOME
COMPANY
NEWS
TECHNOLOGY
R&D
QUALITY
SERVICES
Prenatal
Neonatal
Health Checkup
Rare Disease
Precision Oncology
CONTACT
More
Use tab to navigate through the menu items.
First Korean Case of Renpenning Syndrome with Novel Mutation in PQBP1 Diagnosed by Targeted Exome Sequencing, and Literature Review.
bottom of page