Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy

Articolo pubblicato su J Med Genet 2003;40:473–478

Per leggere il contenuto clicca qui: Articolo 2003