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JOURNAL OF BIOSOCIAL SCIENCE (2000)
Rett syndrome:: a surprising result of mutation in MECP2
J Dragich et al.
HUMAN MOLECULAR GENETICS (2000)
MECP2 mutation in male patients with non-specific X-linked mental retardation
A Orrico et al.
FEBS LETTERS (2000)
Filopodia, spines, and the generation of synaptic diversity
JD Jontes et al.
NEURON (2000)
Neuroligin expressed in nonneuronal cells triggers presynaptic development in contacting axons
P Scheiffele et al.
CELL (2000)
Varieties of repetitive behavior in autism: Comparisons to mental retardation
JW Bodfish et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2000)
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2
A Bolino et al.
NATURE GENETICS (2000)
Prevalence of psychiatric diagnoses in children with mental retardation: data from a population-based study
P Stromme et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2000)
Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation
RJ Gibbons et al.
NATURE GENETICS (2000)
A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation
R Zemni et al.
NATURE GENETICS (2000)