论文信息 - Waardenburg Syndrome: description of two novel mutations in the PAX3 gene, one of which incompletely penetrant - 字舞流文

Waardenburg Syndrome: description of two novel mutations in the PAX3 gene, one of which incompletely penetrant

J. Mazzeu | P. Otto | R. Mingroni-Netto | M. T. Auricchio | Eliete Pardono | R. M. Nascimento | Karina Lezirovitz | P. Iughetti