| No | 記事 | 記事著者 |
|---|
| 1 | Disruption of the ProSAP2 Gene in a t(12;22)(q24.1;q13.3) Is Associated with the 22q13.3 Deletion Syndrome | Maria Clara Bonaglia, Robert Giorda, ... |
| 2 | Mutations in the Sepiapterin Reductase Gene Cause a Novel Tetrahydrobiopterin-Dependent Monoamine-Neurotransmitter Deficiency .. | Luisa Bonate, Beat Thony, Johann M. Penzien, ... |
| 3 | Two Genes That Map to the STSL Locus Cause Sitosterolemia: Genomic Structure and Spectrum of Mutations Involving Sterolin-1 ... | Kangmo Lu, Mi-Hye Lee, Starr Hazard, ... |
