Related Articles
Leigh syndrome T8993C mitochondrial DNA mutation: Heteroplasmy and the first clinical presentation in a Vietnamese family
<em>KRAS</em> mutations and their associations with clinicopathological features and survival in Vietnamese non‑polyp colon cancer patients
FGFR2 mutations and associated clinical observations in two Chinese patients with Crouzon syndrome
Identification of a novel TCOF1 mutation in a Chinese family with Treacher Collins syndrome
Clinical evaluation of RB1 genetic testing reveals novel mutations in Vietnamese patients with retinoblastoma