(Q67484964)
Statements
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 (English)
Collins FA
Murphy DL
Reiss AL
Sims KB
Lewis JG
Karoum F
Zhu D
Maumenee IH