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Search Results - Vonella, Giuseppina
Search Results - Vonella, Giuseppina
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New neurocutaneous syndrome with defect in cell trafficking and melanosome pathway: The future challenge
by
Zannolli, Raffaella
,
Buoni, Sabrina
,
de Santi, Margherita
,
Miracco, Clelia
,
Vonella, Giuseppina
,
Tassini, Maria
,
Vivi, Antonio
,
Viviano, Massimo
,
Rossi, Tiziana
,
Orsi, Alessandra
,
Scarinci, Renato
,
D’Ambrosio, Alfonso
,
Livi, Walter
,
Volterrani, Luca
,
Fois, Alberto
,
Willems, Patrick
,
Hayek, Joseph
Published in
Brain & development (Tokyo. 1979)
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MECP2 deletions and genotype-phenotype correlation in Rett syndrome
by
Scala, Elisa
,
Longo, Ilaria
,
Ottimo, Federica
,
Speciale, Caterina
,
Sampieri, Katia
,
Katzaki, Eleni
,
Artuso, Rosangela
,
Mencarelli, Maria Antonietta
,
D'Ambrogio, Tatiana
,
Vonella, Giuseppina
,
Zappella, Michele
,
Hayek, Giuseppe
,
Battaglia, Agatino
,
Mari, Francesca
,
Renieri, Alessandra
,
Ariani, Francesca
Published in
American journal of medical genetics. Part A
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608: Video EEG: a prognostic method in preterm newborns with neonatal seizures
by
Marchiò, Giuliana
,
Pisani, Francesco
,
Vonella, Giuseppina
Published in
Journal of clinical neuroscience
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Delineation of the phenotype associated with 7q36.1q36.2 deletion: Long QT syndrome, renal hypoplasia and mental retardation
by
Caselli, Rossella
,
Mencarelli, Maria Antonietta
,
Papa, Filomena Tiziana
,
Ariani, Francesca
,
Longo, Ilaria
,
Meloni, Ilaria
,
Vonella, Giuseppina
,
Acampa, Maurizio
,
Auteri, Alberto
,
Vicari, Stefano
,
Orsi, Alessandra
,
Hayek, Giuseppe
,
Renieri, Alessandra
,
Mari, Francesca
Published in
American journal of medical genetics. Part A
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Polydactyly With Ectodermal Defect, Osteopenia, and Mental Delay
by
Zannolli, Raffaella
,
Buoni, Sabrina
,
Viviano, Massimo
,
Macucci, Francesca
,
D'Ambrosio, Alfonso
,
Livi, Walter
,
Mazzei, Maria Antonietta
,
Mazzei, Francesco
,
Sacco, Palmino
,
Volterrani, Luca
,
Vonella, Giuseppina
,
Orsi, Alessandra
,
Zappella, Michele
,
Hayek, Joseph
Published in
Journal of child neurology
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Delineation of the phenotype associated with 7q36.1q36.2 deletion: Long QT syndrome, renal hypoplasia and mental retardation
by
Caselli, Rossella
,
Mencarelli, Maria Antonietta
,
Papa, Filomena Tiziana
,
Ariani, Francesca
,
Longo, Ilaria
,
Meloni, Ilaria
,
Vonella, Giuseppina
,
Acampa, Maurizio
,
Auteri, Alberto
,
Vicari, Stefano
,
Orsi, Alessandra
,
Hayek, Giuseppe
,
Renieri, Alessandra
,
Mari, Francesca
Published in
American Journal of Medical Genetics Part A
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