Magliozzi, Monia
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6

Neonatal diagnosis of ACTA2‐related disease: A case report ..:

Lupo, Viviana ; Di Gregorio, Maria Grazia ; Mastrogiorgio, Gerarda...
American Journal of Medical Genetics Part A.  191 (2023)  4 - p. 1111-1118 , 2023
 
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PrenatalCFAP53-related laterality defect: case report and r..:

Mastromoro, Gioia ; Guadagnolo, Daniele ; Novelli, Antonio...
The Journal of Maternal-Fetal & Neonatal Medicine.  36 (2023)  1 - p. , 2023
 
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A patient with mosaic USP9X gene variant:

Barili, Valeria ; Dall'Asta, Andrea ; Uliana, Vera...
European Journal of Medical Genetics.  65 (2022)  12 - p. 104638 , 2022
 
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11

Cardiovascular Involvement in Pediatric FLNC Variants: A Ca..:

Baban, Anwar ; Alesi, Viola ; Magliozzi, Monia...
Journal of Cardiovascular Development and Disease.  9 (2022)  10 - p. 332 , 2022
 
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12

Clinical and molecular characterizations of 11 new patients..:

Tedesco, Maria Giovanna ; Lonardo, Fortunato ; Ceccarini, Caterina...
American Journal of Medical Genetics Part A.  185 (2021)  4 - p. 1204-1210 , 2021
 
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14

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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