| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Disruptive Technology: CRISPR/Cas-Based Tools and Approaches
|
Patsali, Petros
|
|
2019
|
23 |
2 |
p. 187-200
|
artikel
|
| 2 |
Disruptive Technology: CRISPR/Cas-Based Tools and Approaches
|
Patsali, Petros
|
|
|
23 |
2 |
p. 187-200
|
artikel
|
| 3 |
Gene Therapy for Beta-Hemoglobinopathies: Milestones, New Therapies and Challenges
|
Ghiaccio, Valentina
|
|
2019
|
23 |
2 |
p. 173-186
|
artikel
|
| 4 |
Gene Therapy for Beta-Hemoglobinopathies: Milestones, New Therapies and Challenges
|
Ghiaccio, Valentina
|
|
|
23 |
2 |
p. 173-186
|
artikel
|
| 5 |
Genetic Modifiers of Fetal Haemoglobin in Sickle Cell Disease
|
Menzel, Stephan
|
|
2018
|
23 |
2 |
p. 235-244
|
artikel
|
| 6 |
Genetic Modifiers of Fetal Haemoglobin in Sickle Cell Disease
|
Menzel, Stephan
|
|
|
23 |
2 |
p. 235-244
|
artikel
|
| 7 |
Innovative Therapies for Cystic Fibrosis: The Road from Treatment to Cure
|
Cabrini, Giulio
|
|
2018
|
23 |
2 |
p. 263-279
|
artikel
|
| 8 |
Innovative Therapies for Cystic Fibrosis: The Road from Treatment to Cure
|
Cabrini, Giulio
|
|
|
23 |
2 |
p. 263-279
|
artikel
|
| 9 |
MicroRNAs and Long Non-coding RNAs in Genetic Diseases
|
Finotti, Alessia
|
|
2019
|
23 |
2 |
p. 155-171
|
artikel
|
| 10 |
MicroRNAs and Long Non-coding RNAs in Genetic Diseases
|
Finotti, Alessia
|
|
|
23 |
2 |
p. 155-171
|
artikel
|
| 11 |
Non-invasive Prenatal Testing Using Fetal DNA
|
Breveglieri, Giulia
|
|
2019
|
23 |
2 |
p. 291-299
|
artikel
|
| 12 |
Non-invasive Prenatal Testing Using Fetal DNA
|
Breveglieri, Giulia
|
|
|
23 |
2 |
p. 291-299
|
artikel
|
| 13 |
Omics Studies in Hemoglobinopathies
|
Katsantoni, Eleni
|
|
2019
|
23 |
2 |
p. 223-234
|
artikel
|
| 14 |
Omics Studies in Hemoglobinopathies
|
Katsantoni, Eleni
|
|
|
23 |
2 |
p. 223-234
|
artikel
|
| 15 |
Oxidative Stress in β-Thalassemia
|
Fibach, Eitan
|
|
2018
|
23 |
2 |
p. 245-261
|
artikel
|
| 16 |
Oxidative Stress in β-Thalassemia
|
Fibach, Eitan
|
|
|
23 |
2 |
p. 245-261
|
artikel
|
| 17 |
Rare Opportunities: CRISPR/Cas-Based Therapy Development for Rare Genetic Diseases
|
Papasavva, Panayiota
|
|
2019
|
23 |
2 |
p. 201-222
|
artikel
|
| 18 |
Rare Opportunities: CRISPR/Cas-Based Therapy Development for Rare Genetic Diseases
|
Papasavva, Panayiota
|
|
|
23 |
2 |
p. 201-222
|
artikel
|
| 19 |
Shwachman-Diamond Syndrome: Molecular Mechanisms and Current Perspectives
|
Bezzerri, Valentino
|
|
2018
|
23 |
2 |
p. 281-290
|
artikel
|
| 20 |
Shwachman-Diamond Syndrome: Molecular Mechanisms and Current Perspectives
|
Bezzerri, Valentino
|
|
|
23 |
2 |
p. 281-290
|
artikel
|
| 21 |
Theranostics of Genetic Diseases
|
Gambari, Roberto
|
|
2019
|
23 |
2 |
p. 153-154
|
artikel
|
| 22 |
Theranostics of Genetic Diseases
|
Gambari, Roberto
|
|
|
23 |
2 |
p. 153-154
|
artikel
|
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