| 1 | FS, WT1 |
| Characteristics of testicular dysgenesis syndrome and decreased expression of SRY and SOX9 in Frasier syndrome. | |
| Schumacher V, Gueler B, Looijenga LH, Becker JU, Amann K, Engers R, Dotsch J, Stoop H, Schulz W, Royer-Pokora B. | |
| Mol Reprod Dev 75(9):1484-94. 2008 | |
| 2 | GBGT1, WT1, FS |
| Donor splice-site mutations in WT1 are responsible for Frasier syndrome. | |
| Barbaux S, Niaudet P, Gubler MC, Grunfeld JP, Jaubert F, Kuttenn F, Fekete CN, Souleyreau-Therville N, Thibaud E, Fellous M, McElreavey K. | |
| Nat Genet 17(4):467-70. 1997 | |
| 3 | SLC26A4, FS, WT1 |
| Distinct molecular origins for Denys-Drash and Frasier syndromes. | |
| Poulat F, et al. | |
| Hum Genet 91 : 285-286. 1993 | |