An unusual phenotype of fraiser syndrome due to IVS9 +4C>T mutation in the WT1 gene predominantly male ambiguous genitalia and absence of gonadal dysgenesis

Karla F. S. Melo Regina M Martin; Elaine M. F Costa; Filomena Carvalho; Alexander A Jorge; Ivo J. P Arnhold; Berenice B Mendonça

The Journal of Clinical Endocrinology & Metabolism Bethesda v. 87, n. 6, p. 2500-2505, 2002

Bethesda 2002

Item não circula. Consulte sua biblioteca.(Acessar)