| 1 | SIDDT, TSPYL1 |
| Genetic investigation of the TSPYL1 gene in sudden infant death syndrome. | |
| Hering R, Frade-Martinez R, Bajanowski T, Poets CF, Tschentscher F, Riess O. | |
| Genet Med 8(1):55-8. 2006 | |
| 2 | TSPYL1, SIDDT |
| Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function. | |
| Puffenberger EG, Hu-Lince D, Parod JM, Craig DW, Dobrin SE, Conway AR, Donarum EA, Strauss KA, Dunckley T, Cardenas JF, Melmed KR, Wright CA, Liang W, Stafford P, Flynn CR, Morton DH, Stephan DA. | |
| Proc Natl Acad Sci U S A 101(32):11689-94. Epub 2004 Jul 23. 2004 | |