TY  - GEN
AU  - McConkie-Rosell,A
AU  - Lachiewicz,A M
AU  - Spiridigliozzi,G A
AU  - Tarleton,J
AU  - Schoenwald,S
AU  - Phelan,M C
AU  - Goonewardena,P
AU  - Ding,X
AU  - Brown,W T
TI  - Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome
SN  - 0002-9297
PY  - 1993///1028
KW  - Adult
KW  - Chromosome Mapping
KW  - DNA
KW  - genetics
KW  - Female
KW  - Fragile X Mental Retardation Protein
KW  - Fragile X Syndrome
KW  - Genetic Variation
KW  - Humans
KW  - Male
KW  - Methylation
KW  - Middle Aged
KW  - Nerve Tissue Proteins
KW  - Pedigree
KW  - Phenotype
KW  - Psychological Tests
KW  - RNA-Binding Proteins
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
ER  -