TY  - GEN
AU  - Parrini,E
AU  - Ramazzotti,A
AU  - Dobyns,W B
AU  - Mei,D
AU  - Moro,F
AU  - Veggiotti,P
AU  - Marini,C
AU  - Brilstra,E H
AU  - Dalla Bernardina,B
AU  - Goodwin,L
AU  - Bodell,A
AU  - Jones,M C
AU  - Nangeroni,M
AU  - Palmeri,S
AU  - Said,E
AU  - Sander,J W
AU  - Striano,P
AU  - Takahashi,Y
AU  - Van Maldergem,L
AU  - Leonardi,G
AU  - Wright,M
AU  - Walsh,C A
AU  - Guerrini,R
TI  - Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations
SN  - 1460-2156
PY  - 2006///0803
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Adolescent
KW  - Adult
KW  - Brain
KW  - abnormalities
KW  - Child
KW  - Child, Preschool
KW  - Contractile Proteins
KW  - Ehlers-Danlos Syndrome
KW  - Female
KW  - Filamins
KW  - Fragile X Syndrome
KW  - Genetic Diseases, X-Linked
KW  - Genotype
KW  - Humans
KW  - Hydrocephalus
KW  - Limb Deformities, Congenital
KW  - Magnetic Resonance Imaging
KW  - methods
KW  - Male
KW  - Microcephaly
KW  - Microfilament Proteins
KW  - Middle Aged
KW  - Mutation
KW  - Pedigree
KW  - Phenotype
N1  - Publication Type: Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1093/brain/awl125
ER  -