TY  - GEN
AU  - Winnepenninckx,Birgitta
AU  - Errijgers,Vanessa
AU  - Hayez-Delatte,France
AU  - Reyniers,Edwin
AU  - Frank Kooy,R
TI  - Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: is there a need for routine screening?
SN  - 1098-1004
PY  - 2003///0103
KW  - Alanine
KW  - genetics
KW  - Amino Acid Substitution
KW  - Child, Preschool
KW  - Chromosomal Proteins, Non-Histone
KW  - Chromosomes, Human, X
KW  - CpG Islands
KW  - DNA-Binding Proteins
KW  - Female
KW  - Genetic Carrier Screening
KW  - Genetic Testing
KW  - trends
KW  - Haplotypes
KW  - Humans
KW  - Infant
KW  - Intellectual Disability
KW  - Male
KW  - Methyl-CpG-Binding Protein 2
KW  - Mutation
KW  - Pedigree
KW  - Repressor Proteins
KW  - Rett Syndrome
KW  - Valine
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/humu.10130
ER  -