Search

Author/Creator Hernando‐Davalillo, Cristina

1. Chromosome Microarray Analysis for the Investigation of Deletions in Pediatric Movement Disorders: A Systematic Review of the Literature. Issue 4 (16th March 2023)

Authors:
Soliani, Luca; Alcalá San Martín, Adrián; Balsells, Sol; Hernando‐Davalillo, Cristina; Ortigoza‐Escobar, Juan Darío
Journal:
Movement disorders clinical practice
Issue:
Volume 10:Issue 4(2023)
Page Start:
547
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Expanding the phenotype of X‐linked SSR4–CDG: Connective tissue implications. Issue 2 (21st December 2020)

Authors:
Castiglioni, Claudia; Feillet, François; Barnerias, Christine; Wiedemann, Arnaud; Muchart, Jordi; Cortes, Fanny; Hernando‐Davalillo, Cristina; Montero, Raquel; Dupré, Thierry; Bruneel, Arnaud; Seta, Nathalie; Vuillaumier‐Barrot, Sandrine; Serrano, Mercedes
Journal:
Human mutation
Issue:
Volume 42:Issue 2(2021)
Page Start:
142
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Expanding the phenotype of X‐linked SSR4–CDG: Connective tissue implications. Issue 2 (21st December 2020)

Authors:
Castiglioni, Claudia; Feillet, François; Barnerias, Christine; Wiedemann, Arnaud; Muchart, Jordi; Cortes, Fanny; Hernando‐Davalillo, Cristina; Montero, Raquel; Dupré, Thierry; Bruneel, Arnaud; Seta, Nathalie; Vuillaumier‐Barrot, Sandrine; Serrano, Mercedes
Journal:
Human mutation
Issue:
Volume 42:Issue 2(2021)
Page Start:
142
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗