Orlando, Valeria
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5

A Complex Genomic Rearrangement Resulting in Loss of Functi..:

Orlando, Valeria ; Di Tommaso, Silvia ; Alesi, Viola...
International Journal of Molecular Sciences.  23 (2022)  21 - p. 12900 , 2022
 
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Reciprocal Xp11.4p11.3 microdeletion/microduplication spann..:

Catino, Giorgia ; Genovese, Silvia ; Di Tommaso, Silvia...
American Journal of Medical Genetics Part A.  188 (2022)  6 - p. 1836-1847 , 2022
 
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8p23.1 deletion: Look out for left ventricular hypertrabecu..:

Cicenia, Marianna ; Alesi, Viola ; Orlando, Valeria...
American Journal of Medical Genetics Part A.  188 (2021)  3 - p. 883-895 , 2021
 
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Homozygous HESX1 and COL1A1 Gene Variants in a Boy with Gro..:

Alesi, Viola ; Dentici, Maria Lisa ; Genovese, Silvia...
International Journal of Molecular Sciences.  22 (2021)  2 - p. 750 , 2021
 
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1p36 Deletion Syndrome and the Aorta: A Report of Three New..:

Lodato, Valentina ; Orlando, Valeria ; Alesi, Viola...
Journal of Cardiovascular Development and Disease.  8 (2021)  11 - p. 159 , 2021
 
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PPP1R21‐related syndromic intellectual disability: Report o..:

Loddo, Sara ; Alesi, Viola ; Radio, Francesca Clementina...
American Journal of Medical Genetics Part A.  182 (2020)  12 - p. 3014-3022 , 2020
 
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14

Atypical 7q11.23 deletions excluding ELN gene result in Wil..:

Alesi, Viola ; Loddo, Sara ; Orlando, Valeria...
American Journal of Medical Genetics Part A.  185 (2020)  1 - p. 242-249 , 2020
 
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A heterozygous, intragenic deletion of CNOT2 recapitulates ..:

Alesi, Viola ; Loddo, Sara ; Calì, Federica...
American Journal of Medical Genetics Part A.  179 (2019)  8 - p. 1615-1621 , 2019
 
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