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Rett syndrome: Lack of association with fragile site Xp22 and strategy for genetic mapping of X-linked new mutations

✍ Scribed by Romeo, Giovanni ;Archidiacono, Nicoletta ;Ferlini, Alessandra ;Rocchi, Mariano ;Opitz, John M. ;Reynolds, James F.


Publisher
John Wiley and Sons
Year
1986
Tongue
English
Weight
253 KB
Volume
25
Category
Article
ISSN
0148-7299

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