- Neuronal migration mechanisms in development and disease.
- A novel sex determination system in a close relative of the house mouse.
- Nup153 and megator define transcriptionally active regions in the Drosophila genome.
French Institute for Health and Medical Research - INSERM
Marseilles University Hospital
INSERM U910 : Team Genetics of Neuromuscular disorders
INSERM U910 : Team Genetics, Patterning and Cardiac Diseases
French Rett Syndrome Association - AFSR
International Rett Syndrome Foundation - IRSF
Polymicrogyria discussion group (Yahoo)
Network on lissencephaly and other brain diseases
Lissencephaly contact group (Royaume-Uni)
Federation of Orphan Diseases - FMO
Federation for Brain Research - FRC
X-linked mental retardation association - Xtraordinaire
Rare diseases and orphan drugs - ORPHANET
Online Inheritance in Man - OMIM
Human Gene Mutation Database - HGMD
MECP2 mutation database - Australia
MECP2 mutation database - United Kingdom
RettSearch - Clinical research for Rett syndrome
EuroRETT - European Network on Rett syndrome
Human Genome Resources at NCBI
ORPHA SCHOOL - On-line teaching
Society for Neuroscience - France
Society for Neuroscience - USA
The American Association on Intellectual and Developmental Disabilities - AAIDD