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Identification of three novel mutations in the CHD7 gene in patients with clinical signs of typical or atypical CHARGE syndrome

✍ Scribed by Angela Michelucci; Paolo Ghirri; Paola Iacopetti; Maria Elena Conidi; Antonella Fogli; Fulvia Baldinotti; Sara Lunardi; Francesca Forli; Francesca Moscuzza; Stefano Berrettini; Antonio Boldrini; Paolo Simi; Silvia Pellegrini


Book ID
116565767
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
265 KB
Volume
74
Category
Article
ISSN
0165-5876

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