000 01449 a2200445 4500
005 20250513033030.0
264 0 _c19951208
008 199512s 0 0 eng d
022 _a1061-4036
024 7 _a10.1038/ng1195-331
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aReiss, A L
245 0 0 _aContribution of the FMR1 gene mutation to human intellectual dysfunction.
_h[electronic resource]
260 _bNature genetics
_cNov 1995
300 _a331-4 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAdolescent
650 0 4 _aCase-Control Studies
650 0 4 _aChild
650 0 4 _aDosage Compensation, Genetic
650 0 4 _aFemale
650 0 4 _aFragile X Mental Retardation Protein
650 0 4 _aFragile X Syndrome
_xgenetics
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aIntelligence
_xgenetics
650 0 4 _aIntelligence Tests
650 0 4 _aMutation
650 0 4 _aNerve Tissue Proteins
_xgenetics
650 0 4 _aParents
650 0 4 _aRNA-Binding Proteins
650 0 4 _aRegression Analysis
650 0 4 _aRepetitive Sequences, Nucleic Acid
700 1 _aFreund, L S
700 1 _aBaumgardner, T L
700 1 _aAbrams, M T
700 1 _aDenckla, M B
773 0 _tNature genetics
_gvol. 11
_gno. 3
_gp. 331-4
856 4 0 _uhttps://doi.org/10.1038/ng1195-331
_zAvailable from publisher's website
999 _c7580901
_d7580901