| Title | Date | Type | Setname | ||
|---|---|---|---|---|---|
| 1 |
 | Characterization of intronic variants in BRCA1 and BRCA2 | 2000-08 | Text | ir_etd |
| 2 |
 | Identification of OPA1 Mutations in Autosomal Dominant Optic Atrophy (ADOA): Toward the Role of the Mitochondria in ADOA | 2004-03-31 | Text | ehsl_novel_nam |
| 3 |
 | Infection-dependent phenotypes in MHC-congenic mice are not due to MHC: can we trust congenic animals? | 2004 | Text | ir_uspace |
| 4 |
 | Molecular genetics of the long QT syndrome | 1995-12 | Text | ir_etd |
| 5 |
 | Multiple transcripts from the Antennapedia gene of Drosophila melanogaster | 1986 | Text | ir_uspace |
| 6 |
 | Myotonia congenita-associated chloride channelopathies: mutations, function, and structure. | 1999-12 | Text | ir_etd |
| 7 |
 | The nuclear actin-related proteins, Arp7 and Arp9: connecting ARP hetertodimerization to the regulation of chromatin remodling. | 2004-08 | Text | ir_etd |
| 8 |
 | Targeted mutagenesis by homologous recombination in D. melanogaster | 2002 | Text | ir_uspace |
| 9 |
 | Transcriptional regulation by the ACE2 and SWI5 activators in yeast | 1994-12 | Text | ir_etd |