000 01463 a2200457 4500
005 20250513064952.0
264 0 _c19931028
008 199310s 0 0 eng d
022 _a0002-9297
040 _aNLM
_beng
_cNLM
100 1 _aMcConkie-Rosell, A
245 0 0 _aEvidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome.
_h[electronic resource]
260 _bAmerican journal of human genetics
_cOct 1993
300 _a800-9 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAdult
650 0 4 _aChromosome Mapping
650 0 4 _aDNA
_xgenetics
650 0 4 _aFemale
650 0 4 _aFragile X Mental Retardation Protein
650 0 4 _aFragile X Syndrome
_xgenetics
650 0 4 _aGenetic Variation
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMethylation
650 0 4 _aMiddle Aged
650 0 4 _aNerve Tissue Proteins
_xgenetics
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aPsychological Tests
650 0 4 _aRNA-Binding Proteins
700 1 _aLachiewicz, A M
700 1 _aSpiridigliozzi, G A
700 1 _aTarleton, J
700 1 _aSchoenwald, S
700 1 _aPhelan, M C
700 1 _aGoonewardena, P
700 1 _aDing, X
700 1 _aBrown, W T
773 0 _tAmerican journal of human genetics
_gvol. 53
_gno. 4
_gp. 800-9
999 _c8213102
_d8213102