Related Articles
Occult macular dystrophy in an Italian family carrying a mutation in the RP1L1 gene
Potential genetic damage to nematode offspring following exposure to triclosan during pregnancy
Successful preimplantation genetic diagnosis by targeted next-generation sequencing on an ion torrent personal genome machine platform
Characterization of a novel receptor mutation A↷T at exon 4 in complete androgen insensitivity syndrome and a carrier sibling via bidirectional polymorphism sequence analysis
Successful clinical application of pre‑implantation genetic diagnosis for infantile neuroaxonal dystrophy