TY  - GEN
AU  - Chen,R M
AU  - Lupski,J R
AU  - Greenberg,F
AU  - Lewis,R A
TI  - Ophthalmic manifestations of Smith-Magenis syndrome
SN  - 0161-6420
PY  - 1996///0822
KW  - Abnormalities, Multiple
KW  - diagnosis
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 17
KW  - genetics
KW  - Corneal Diseases
KW  - Eye Diseases
KW  - Female
KW  - Humans
KW  - Infant
KW  - Intellectual Disability
KW  - Iris Diseases
KW  - Karyotyping
KW  - Male
KW  - Myopia
KW  - Strabismus
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review
UR  - https://doi.org/10.1016/s0161-6420(96)30563-0
ER  -