(Q41379988)
Statements
1 reference
Rett syndrome: lack of association with fragile site Xp22 and strategy for genetic mapping of X-linked new mutations (English)
1 reference
Romeo G
1 reference
Archidiacono N
1 reference
Ferlini A
1 reference
Rocchi M
1 reference
1 January 1986
1 reference
1 reference