TY  - GEN
AU  - Chiurazzi,P
AU  - de Graaff,E
AU  - Ng,J
AU  - Verkerk,A J
AU  - Wolfson,S
AU  - Fisch,G S
AU  - Kozak,L
AU  - Neri,G
AU  - Oostra,B A
TI  - No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome
SN  - 0148-7299
PY  - 1994///1116
KW  - Child
KW  - Child, Preschool
KW  - DNA Mutational Analysis
KW  - Fragile X Mental Retardation Protein
KW  - Fragile X Syndrome
KW  - genetics
KW  - Genes
KW  - Genotype
KW  - Humans
KW  - Intellectual Disability
KW  - etiology
KW  - Male
KW  - Mutation
KW  - Nerve Tissue Proteins
KW  - biosynthesis
KW  - Pedigree
KW  - Phenotype
KW  - RNA, Messenger
KW  - metabolism
KW  - RNA-Binding Proteins
KW  - X Chromosome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.1320510405
ER  -