TY  - GEN
AU  - Ross,M E
AU  - Allen,K M
AU  - Srivastava,A K
AU  - Featherstone,T
AU  - Gleeson,J G
AU  - Hirsch,B
AU  - Harding,B N
AU  - Andermann,E
AU  - Abdullah,R
AU  - Berg,M
AU  - Czapansky-Bielman,D
AU  - Flanders,D J
AU  - Guerrini,R
AU  - Motté,J
AU  - Mira,A P
AU  - Scheffer,I
AU  - Berkovic,S
AU  - Scaravilli,F
AU  - King,R A
AU  - Ledbetter,D H
AU  - Schlessinger,D
AU  - Dobyns,W B
AU  - Walsh,C A
TI  - Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain
SN  - 0964-6906
PY  - 1997///0715
KW  - Cerebral Cortex
KW  - abnormalities
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 2
KW  - genetics
KW  - Dosage Compensation, Genetic
KW  - Epilepsy
KW  - etiology
KW  - Female
KW  - Genetic Linkage
KW  - Humans
KW  - Hybrid Cells
KW  - In Situ Hybridization, Fluorescence
KW  - Karyotyping
KW  - Male
KW  - Pedigree
KW  - Phenotype
KW  - Restriction Mapping
KW  - Sex Chromosome Aberrations
KW  - Translocation, Genetic
KW  - X Chromosome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1093/hmg/6.4.555
ER  -