Sfoglia per Correlatore
Mostrati risultati da 1 a 4 di 4
Absolute telomere length in Hereditary Hemorrhagic Telangiectasia
2021/2022 NARDIELLO, CHANTAL
From Sanger to NGS: sequencing methods to detect GBA variants in patients with Parkinson's Disease.
2020/2021 CUCONATO, GIADA
Genetic Studies on a Rare Mendelian Disease: Shwachman-Diamond Syndrome
2021/2022 FORONI, SELENA
Hereditary haemorrhagic telangiectasia: mutation analysis and TaqMan® validation of preliminary results in circulating miRNAs studies
2019/2020 SBALCHIERO, ANNA
| collection | Anno | Titolo | Autore | file(s) |
|---|---|---|---|---|
| Lauree Magistrali | 2021/2022 | Absolute telomere length in Hereditary Hemorrhagic Telangiectasia | NARDIELLO, CHANTAL | |
| Lauree Magistrali | 2020/2021 | From Sanger to NGS: sequencing methods to detect GBA variants in patients with Parkinson's Disease. | CUCONATO, GIADA | |
| Lauree Magistrali | 2021/2022 | Genetic Studies on a Rare Mendelian Disease: Shwachman-Diamond Syndrome | FORONI, SELENA | |
| Lauree Magistrali | 2019/2020 | Hereditary haemorrhagic telangiectasia: mutation analysis and TaqMan® validation of preliminary results in circulating miRNAs studies | SBALCHIERO, ANNA |
Mostrati risultati da 1 a 4 di 4
Legenda icone
- file ad accesso aperto
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile