000 01482 a2200457 4500
005 20250511214921.0
264 0 _c19910207
008 199102s 0 0 eng d
022 _a0028-3878
024 7 _a10.1212/wnl.41.1.80
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBrunner, H G
245 0 0 _aGenetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathy.
_h[electronic resource]
260 _bNeurology
_cJan 1991
300 _a80-4 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aChild
650 0 4 _aChromosomes, Human, Pair 17
650 0 4 _aChromosomes, Human, Pair 19
650 0 4 _aDNA
_xanalysis
650 0 4 _aElectromyography
650 0 4 _aFemale
650 0 4 _aGenetic Linkage
650 0 4 _aHereditary Sensory and Motor Neuropathy
_xcomplications
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMyotonic Dystrophy
_xcomplications
650 0 4 _aPedigree
650 0 4 _aPhysical Examination
700 1 _aSpaans, F
700 1 _aSmeets, H J
700 1 _aCoerwinkel-Driessen, M
700 1 _aHulsebos, T
700 1 _aWieringa, B
700 1 _aRopers, H H
773 0 _tNeurology
_gvol. 41
_gno. 1
_gp. 80-4
856 4 0 _uhttps://doi.org/10.1212/wnl.41.1.80
_zAvailable from publisher's website
999 _c1991484
_d1991484