Philippe Loget

Chromosome Abnormalities and Genetic Counseling

Cerebral cortex expansion and folding: what have we learned?

Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans

Metazoan MicroRNAs

FGFR3 targeting strategies for achondroplasia

MicroRNA therapeutics: towards a new era for the management of cancer and other diseases

Health Supervision for Children With Down Syndrome

The Fibroblast Growth Factor signaling pathway

Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals

New Insight on FGFR3-Related Chondrodysplasias Molecular Physiopathology Revealed by Human Chondrocyte Gene Expression Profiling

Twelve new patients with 13q deletion syndrome: Genotype–phenotype analyses in progress

Neuropathological phenotype of a distinct form of lissencephaly associated with mutations in TUBA1A