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Rizzo, Caterina Lo
578
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Online (577)
Print (1)
Mediatypes
Articles (Online) (477)
Articles (Print) (1)
Bookchapter (Online) (14)
OpenAccess-fulltext (86)
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1
A genome-wide association study for survival from a multi-c..:
Minnai, Francesca
;
Biscarini, Filippo
;
Esposito, Martina
...
Scientific Reports. 14 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1038/..
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2
Ultra-rare RTEL1 gene variants associate with acute severit..:
Bergantini, Laura
;
Baldassarri, Margherita
;
d'Alessandro, Miriana
...
Respiratory Research. 24 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
3
An explainable model of host genetic interactions linked to..:
Onoja, Anthony
;
Picchiotti, Nicola
;
Fallerini, Chiara
...
Communications Biology. 5 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1038/..
?
4
Expanding the clinical spectrum associated with the PACS1 p..:
Bruno, Lucia Pia
;
Doddato, Gabriella
;
Baldassarri, Margherita
...
American Journal of Medical Genetics Part A. 191 (2022) 1 - p. 284-288 , 2022
Link:
https://doi.org/10.1002/..
?
5
Corrigendum: Exome Sequencing in BRCA1-2 Candidate Familias..:
Doddato, Gabriella
;
Valentino, Floriana
;
Giliberti, Annarita
...
Frontiers in Oncology. 11 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
6
Sporadic hereditary motor and sensory neuropathies: Advance..:
Fallerini, Chiara
;
Carignani, Giulia
;
Capoccitti, Giorgio
...
Journal of the Neurological Sciences. 359 (2015) 1-2 - p. 409-417 , 2015
Link:
https://doi.org/10.1016/..
?
7
Interstitial 22q13 deletions not involving SHANK3 gene: A n..:
Disciglio, Vittoria
;
Rizzo, Caterina Lo
;
Mencarelli, Maria Antonietta
...
American Journal of Medical Genetics Part A. 164 (2014) 7 - p. 1666-1676 , 2014
Link:
https://doi.org/10.1002/..
?
8
PP-207. Evidence of oxidative stress in Beckwith Wiedemann ..:
Rizzo, Caterina Lo
;
Anichini, Cecilia
;
Rodriguez, Antonello
...
Early Human Development. 86 (2010) - p. S100 , 2010
Link:
https://doi.org/10.1016/..
?
9
PP-209. Beckwith Wiedemann Syndrome: Administration of pota..:
Rizzo, Caterina Lo
;
Anichini, Cecilia
;
Proietti, Fabrizio
...
Early Human Development. 86 (2010) - p. S100-S101 , 2010
Link:
https://doi.org/10.1016/..
?
10
MET is a new confirmed gene responsible for familial distal..:
Maffeo, Debora
;
Carrer, Anna
;
Rina, Angela
...
EMBO Molecular Medicine. 16 (2024) 4 - p. 720-722 , 2024
Link:
https://doi.org/10.1038/..
?
11
Correction to: High rate of HDR in gene editing of p.(Thr15..:
Croci, Susanna
;
Carriero, Miriam Lucia
;
Capitani, Katia
...
European Journal of Human Genetics. 32 (2023) 1 - p. 134-134 , 2023
Link:
https://doi.org/10.1038/..
?
12
An Example of Neuro-Glial Commitment and Differentiation of..:
Al Sammarraie, Sura Hilal Ahmed
;
Aprile, Domenico
;
Meloni, Ilaria
...
Cells. 12 (2023) 7 - p. 977 , 2023
Link:
https://doi.org/10.3390/..
?
13
Understanding the new BRD4‐related syndrome: Clinical and g..:
Jouret, Guillaume
;
Heide, Solveig
;
Sorlin, Arthur
...
Clinical Genetics. 102 (2022) 2 - p. 117-122 , 2022
Link:
https://doi.org/10.1111/..
?
14
Exome Sequencing in BRCA1-2 Candidate Familias: The Contrib..:
Doddato, Gabriella
;
Valentino, Floriana
;
Giliberti, Annarita
...
Frontiers in Oncology. 11 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
15
IQSEC2 disorder: A new disease entity or a Rett spectrum co..:
Lopergolo, Diego
;
Privitera, Flavia
;
Castello, Giuseppe
...
Clinical Genetics. 99 (2021) 3 - p. 462-474 , 2021
Link:
https://doi.org/10.1111/..
1-15