Collection's Items (Sorted by Submit Date in Descending order): 1 to 4 of 4
| Issue Date | Title | Author(s) | Type | Access Type |
| Apr-2004 | Homozygosity mapping of a third Joubert syndrome locus to 6q23. | Lagier-Tourenne, C.; Boltshauser, E.; Breivik, N.; Gribaa, M.; Bétard, C.; Barbot, C.; Koenig, M. | article |  |
| Aug-1999 | Two pairs of proven monozygotic twins discordant for familial amyloid neuropathy (FAP) TTR Met 30. | MUNAR‐QUES, M.; PEDROSA, J.L.; COELHO, T.; GUSMAO, L.; SERUCA, R.; AMORIM, A.; SEQUEIROS, J. | article | |
| Mar-2007 | Identification of a new mtDNA mutation (14724G>A) associated with mitochondrial leukoencephalopathy | PEREIRA, C.; NOGUEIRA, C.; BARBOT, C.; TESSA, A.; SOARES, C.; FATTORI, F.; GUIMARÃES, A.; SANTORELLI, F.M.; VILARINHO, L. | article | |
| Sep-2007 | Changes in the Clonal Nature and Antibiotic Resistance Profiles of Methicillin-Resistant Staphylococcus aureus Isolates Associated with Spread of the EMRSA-15 Clone in a Tertiary Care Portuguese Hospital | Amorim, M.; Faria, N.; Oliveira, D.; Vasconcelos, C.; Cabeda, J.; Mendes, A.; Calado, E.; Castro, A.; Ramos, M.; Amorim, J.; Lencastre, H. | article | |
Collection's Items (Sorted by Submit Date in Descending order): 1 to 4 of 4
