LIEHR, THOMAS
LIEHR, THOMAS
DIPARTIMENTO DI MEDICINA MOLECOLARE
An interstitial 4q31.21q31.22 microdeletion associated with developmental delay: case report and literature review.
2014-01-01 Vlaikou, Am; Manolakos, E; Noutsopoulos, D; Markopoulos, G; Liehr, Thomas; Vetro, Annalisa; Ziegler, MARTIN BURKHARD ANDREAS; Weise, A; Kreskowski, K; Papoulidis, I; Thomaidis, L; Syrrou, M.
Complex rearrangement involving three chromosomes, four breakpoints and a 2.7-Mb deletion in the 18q segment observed in a girl with mild learning difficulties
2016-01-01 Kontodiou, M. 1; Daskalakis, G; Vetro, Annalisa; Paspaliaris, V.; Papaioannou, G; Dagklis, T; Tsakiridis, I; Ziegler, MARTIN BURKHARD ANDREAS; Liehr, Thomas; Thomaidis, L; Papoulidis, I; Manolakos,
Insertional translocation involving an additional nonchromothriptic chromosome in constitutional chromothripsis: Rule or exception?
2019-01-01 Kurtas, N. E.; Xumerle, L.; Giussani, U.; Pansa, A.; Cardarelli, L.; Bertini, V.; Valetto, A.; Liehr, T.; Clara Bonaglia, M.; Errichiello, E.; Delledonne, M.; Zuffardi, O.
Small supernumerary marker chromosomes: A legacy of trisomy rescue?
2019-01-01 Kurtas, N. E.; Xumerle, L.; Leonardelli, L.; Delledonne, M.; Brusco, A.; Chrzanowska, K.; Schinzel, A.; Larizza, D.; Guerneri, S.; Natacci, F.; Bonaglia, M. C.; Reho, P.; Manolakos, E.; Mattina, T.; Soli, F.; Provenzano, A.; Al-Rikabi, A. H.; Errichiello, E.; Nazaryan-Petersen, L.; Giglio, S.; Tommerup, N.; Liehr, T.; Zuffardi, O.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| An interstitial 4q31.21q31.22 microdeletion associated with developmental delay: case report and literature review. | 1-gen-2014 | Vlaikou, Am; Manolakos, E; Noutsopoulos, D; Markopoulos, G; Liehr, Thomas; Vetro, Annalisa; Ziegler, MARTIN BURKHARD ANDREAS; Weise, A; Kreskowski, K; Papoulidis, I; Thomaidis, L; Syrrou, M. | |
| Complex rearrangement involving three chromosomes, four breakpoints and a 2.7-Mb deletion in the 18q segment observed in a girl with mild learning difficulties | 1-gen-2016 | Kontodiou, M. 1; Daskalakis, G; Vetro, Annalisa; Paspaliaris, V.; Papaioannou, G; Dagklis, T; Tsakiridis, I; Ziegler, MARTIN BURKHARD ANDREAS; Liehr, Thomas; Thomaidis, L; Papoulidis, I; Manolakos, | |
| Insertional translocation involving an additional nonchromothriptic chromosome in constitutional chromothripsis: Rule or exception? | 1-gen-2019 | Kurtas, N. E.; Xumerle, L.; Giussani, U.; Pansa, A.; Cardarelli, L.; Bertini, V.; Valetto, A.; Liehr, T.; Clara Bonaglia, M.; Errichiello, E.; Delledonne, M.; Zuffardi, O. | |
| Small supernumerary marker chromosomes: A legacy of trisomy rescue? | 1-gen-2019 | Kurtas, N. E.; Xumerle, L.; Leonardelli, L.; Delledonne, M.; Brusco, A.; Chrzanowska, K.; Schinzel, A.; Larizza, D.; Guerneri, S.; Natacci, F.; Bonaglia, M. C.; Reho, P.; Manolakos, E.; Mattina, T.; Soli, F.; Provenzano, A.; Al-Rikabi, A. H.; Errichiello, E.; Nazaryan-Petersen, L.; Giglio, S.; Tommerup, N.; Liehr, T.; Zuffardi, O. |