TY  - GEN
AU  - Pinard,J M
AU  - Motte,J
AU  - Chiron,C
AU  - Brian,R
AU  - Andermann,E
AU  - Dulac,O
TI  - Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene
SN  - 0022-3050
PY  - 1994///0909
KW  - Adolescent
KW  - Adult
KW  - Cerebral Cortex
KW  - abnormalities
KW  - Child
KW  - Congenital Abnormalities
KW  - diagnosis
KW  - Epilepsy
KW  - etiology
KW  - Female
KW  - Genes, Dominant
KW  - genetics
KW  - Genetic Counseling
KW  - Genetic Linkage
KW  - Humans
KW  - Infant
KW  - Intellectual Disability
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Pedigree
KW  - Sex Chromosome Aberrations
KW  - X Chromosome
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1136/jnnp.57.8.914
ER  -