TY  - GEN
AU  - Collins,F A
AU  - Murphy,D L
AU  - Reiss,A L
AU  - Sims,K B
AU  - Lewis,J G
AU  - Freund,L
AU  - Karoum,F
AU  - Zhu,D
AU  - Maumenee,I H
AU  - Antonarakis,S E
TI  - Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes
SN  - 0148-7299
PY  - 1993///0927
KW  - Adolescent
KW  - Blindness
KW  - genetics
KW  - Chromosome Deletion
KW  - Female
KW  - Heterozygote
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Monoamine Oxidase
KW  - deficiency
KW  - Myoclonus
KW  - Phenotype
KW  - Stereotyped Behavior
KW  - Syndrome
KW  - X Chromosome
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1002/ajmg.1320420126
ER  -