Related Articles
A family with hypothyroidism caused by fatty acid synthase and apolipoprotein B receptor mutations
Exome sequencing reveals novel IRXI mutation in congenital heart disease
Whole exome sequencing identifies novel candidate mutations in a Chinese family with left ventricular noncompaction
Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis
Mutation analysis of the genes associated with anterior segment dysgenesis, microcornea and microphthalmia in 257 patients with glaucoma