E-LIB Suche - Ergebnisse für: Rizzo, Caterina Lo

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/..

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

Exome Sequencing in 200 Intellectual Disability/Autistic Pa..:

Valentino, Floriana ; Bruno, Lucia Pia ; Doddato, Gabriella...
Brain Sciences. 11 (2021) 7 - p. 936 , 2021

Link: https://doi.org/10.3390/..