000 01142 a2200349 4500
005 20250513085141.0
264 0 _c19960321
008 199603s 0 0 eng d
022 _a0173-0835
024 7 _a10.1002/elps.11501601282
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHummerich, H
245 0 0 _aTrinucleotide repeat expansion and human disease.
_h[electronic resource]
260 _bElectrophoresis
_cSep 1995
300 _a1698-704 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
650 0 4 _aAge of Onset
650 0 4 _aChromosome Fragile Sites
650 0 4 _aChromosome Fragility
650 0 4 _aFemale
650 0 4 _aGenetic Diseases, Inborn
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMyotonic Dystrophy
_xgenetics
650 0 4 _aNerve Degeneration
650 0 4 _aSex Characteristics
650 0 4 _aSyndrome
650 0 4 _aTrinucleotide Repeats
700 1 _aLehrach, H
773 0 _tElectrophoresis
_gvol. 16
_gno. 9
_gp. 1698-704
856 4 0 _uhttps://doi.org/10.1002/elps.11501601282
_zAvailable from publisher's website
999 _c8581419
_d8581419