Related Articles
Confirmation of CLIM2/LMX1B interaction by yeast two-hybrid screening and analysis of its involvement in nail-patella syndrome
Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping
Five cases of paroxysmal kinesigenic dyskinesia by genetic diagnosis
Identification of two novel mutations in the <em>PLCD1</em> gene in Chinese patients with hereditary leukonychia
Nail‑Patella syndrome with early onset end‑stage renal disease in a child with a novel heterozygous missense mutation in the LMX1B homeodomain: A case report