To read in august...

- Role of Olig1 and Olig2 in Down syndrome.

- TUBA1A mutations cause wide spectrum lissencephaly.

- Cell cloning-based transcriptome analysis in Rett patients.

Our selection of links


Institutions

French Institute for Health and Medical Research - INSERM

Aix-Marseille University

"La Timone" Medical School

Marseilles University Hospital

INSERM - Knowledge base

French Ministery of Research

Institute For Rare Diseases

INSERM U910 : Team Genetics of Neuromuscular disorders

INSERM U910 : Team Genetics, Patterning and Cardiac Diseases


Associations

French Rett Syndrome Association - AFSR

International Rett Syndrome Foundation - IRSF

Rett Syndrome Europe - RSE

Polymicrogyria discussion group (Yahoo)

Network on lissencephaly and other brain diseases

Lissencephaly contact group (Royaume-Uni)

Federation of Orphan Diseases - FMO

Rare diseases alliance

Federation for Brain Research - FRC

X-linked mental retardation association - Xtraordinaire


Genetic diseases

Rare diseases and orphan drugs - ORPHANET

Online Inheritance in Man - OMIM

Human Gene Mutation Database - HGMD

Genatlas

MECP2 mutation database - Australia

MECP2 mutation database - United Kingdom

RettSearch - Clinical research for Rett syndrome

EuroRETT - European Network on Rett syndrome


Human Genetics

Human chromosome launchpad

Human Genome Central

Human Genome Resources at NCBI

Tools of molecular genetics

ORPHA SCHOOL - On-line teaching


Brain

Medical images database

Virtual hospital, brain pages

Brain atlas

Society for Neuroscience - France

Society for Neuroscience - USA

The American Association on Intellectual and Developmental Disabilities - AAIDD


Local links

City of Marseilles

Regional council

Marseille tourist office

Public transportation in Marseille

Marseille Provence Airport

Self-service bikes in Marseille