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 |