TY  - GEN
AU  - Donzel-Javouhey,Anne
AU  - Thauvin-Robinet,Christel
AU  - Cusin,Veronica
AU  - Madinier,Nathalie
AU  - Manceau,Eric
AU  - Dipanda,Dominique
AU  - Dulieu,Véronique
AU  - Mugneret,Francine
AU  - Huet,Frédéric
AU  - Teyssier,Jean-Raymond
AU  - Faivre,Laurence
TI  - A new cohort of MECP2 mutation screening in unexplained mental retardation: careful re-evaluation is the best indicator for molecular diagnosis
SN  - 1552-4825
PY  - 2006///0928
KW  - Base Sequence
KW  - Cohort Studies
KW  - DNA
KW  - genetics
KW  - Female
KW  - Genetic Testing
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Methyl-CpG-Binding Protein 2
KW  - Mutation
KW  - Phenotype
KW  - Rett Syndrome
N1  - Publication Type: Letter; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.a.31314
ER  -