1)
Male Rett Syndrome patient with mosaic MECP2 mutation.
(World Rett Syndrome congress, Parigi, Francia,
10-13 ottobre 2008)
2)
Congenital Rett Syndrome Variant (World Rett Syndrome congress,
Parigi, Francia, 10-13 ottobre 2008)
3)
FOXG1 is responsible for the Congenital Variant of Rett Syndrome
(ASHG 2008, Philadelphia, Pennsylvania, USA, 11-15 novembre 2008)
4)
Il gene FOXG1 è
responsabile della variante congenita della sindrome di Rett
(Congresso nazionale sigu 2008, Genova, Italia, 23-25 novembre 2008)
5)
Congenital variant of Rett syndrome due to the FOXG1 gene (ESHG
2009, Vienna, Austria, 23-26 maggio 2009)
6)
Diagnostic flow-chart for Rett syndrome (1st European Congress on
Rett Syndrome, Milano, Italia, 5-7 giugno 2009.
7) A
novel mild phenotype associated with FOXG1 gene (ESHG 2010,
Gothenburg, Sweden, 12-15 giugno 2010)
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