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3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination

✍ Scribed by Palumbo, Orazio; D'Agruma, Leonardo; Minenna, Adelaide Franca; Palumbo, Pietro; Stallone, Raffaella; Palladino, Teresa; Zelante, Leopoldo; Carella, Massimo


Book ID
125467545
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
773 KB
Volume
516
Category
Article
ISSN
0378-1119

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