TY  - GEN
AU  - Jen,Joanna C
AU  - Chan,Wai-Man
AU  - Bosley,Thomas M
AU  - Wan,Jijun
AU  - Carr,Janai R
AU  - Rüb,Udo
AU  - Shattuck,David
AU  - Salamon,Georges
AU  - Kudo,Lili C
AU  - Ou,Jing
AU  - Lin,Doris D M
AU  - Salih,Mustafa A M
AU  - Kansu,Tülay
AU  - Al Dhalaan,Hesham
AU  - Al Zayed,Zayed
AU  - MacDonald,David B
AU  - Stigsby,Bent
AU  - Plaitakis,Andreas
AU  - Dretakis,Emmanuel K
AU  - Gottlob,Irene
AU  - Pieh,Christina
AU  - Traboulsi,Elias I
AU  - Wang,Qing
AU  - Wang,Lejin
AU  - Andrews,Caroline
AU  - Yamada,Koki
AU  - Demer,Joseph L
AU  - Karim,Shaheen
AU  - Alger,Jeffry R
AU  - Geschwind,Daniel H
AU  - Deller,Thomas
AU  - Sicotte,Nancy L
AU  - Nelson,Stanley F
AU  - Baloh,Robert W
AU  - Engle,Elizabeth C
TI  - Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis
SN  - 1095-9203
PY  - 2004///0701
KW  - Adult
KW  - Alternative Splicing
KW  - Amino Acid Motifs
KW  - Amino Acid Sequence
KW  - Axons
KW  - physiology
KW  - Evoked Potentials, Motor
KW  - Evoked Potentials, Somatosensory
KW  - Female
KW  - Functional Laterality
KW  - Genetic Linkage
KW  - Humans
KW  - In Situ Hybridization
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Medulla Oblongata
KW  - growth & development
KW  - Microsatellite Repeats
KW  - Molecular Sequence Data
KW  - Morphogenesis
KW  - Mutation
KW  - Neural Pathways
KW  - Ophthalmoplegia
KW  - genetics
KW  - Pedigree
KW  - Protein Structure, Tertiary
KW  - Receptors, Cell Surface
KW  - Receptors, Immunologic
KW  - chemistry
KW  - Reverse Transcriptase Polymerase Chain Reaction
KW  - Rhombencephalon
KW  - Scoliosis
KW  - Sequence Analysis, DNA
KW  - Syndrome
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/10.1126/science.1096437
ER  -