TY  - GEN
AU  - Hargrave,M
AU  - James,K
AU  - Nield,K
AU  - Toomes,C
AU  - Georgas,K
AU  - Sullivan,T
AU  - Verzijl,H T
AU  - Oley,C A
AU  - Little,M
AU  - De Jonghe,P
AU  - Kwon,J M
AU  - Kremer,H
AU  - Dixon,M J
AU  - Timmerman,V
AU  - Yamada,T
AU  - Koopman,P
TI  - Fine mapping of the neurally expressed gene SOX14 to human 3q23, relative to three congenital diseases
SN  - 0340-6717
PY  - 2000///0614
KW  - Amino Acid Sequence
KW  - Animals
KW  - Blepharophimosis
KW  - genetics
KW  - Blepharoptosis
KW  - Charcot-Marie-Tooth Disease
KW  - Chick Embryo
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 3
KW  - Eye Abnormalities
KW  - Genetic Testing
KW  - High Mobility Group Proteins
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Mice
KW  - Mobius Syndrome
KW  - Molecular Sequence Data
KW  - Mutation
KW  - SOXB2 Transcription Factors
KW  - Sequence Homology, Amino Acid
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/10.1007/s004390000266
ER  -