TY  - GEN
AU  - Brunner,H G
AU  - Spaans,F
AU  - Smeets,H J
AU  - Coerwinkel-Driessen,M
AU  - Hulsebos,T
AU  - Wieringa,B
AU  - Ropers,H H
TI  - Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathy
SN  - 0028-3878
PY  - 1991///0207
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Chromosomes, Human, Pair 17
KW  - Chromosomes, Human, Pair 19
KW  - DNA
KW  - analysis
KW  - Electromyography
KW  - Female
KW  - Genetic Linkage
KW  - Hereditary Sensory and Motor Neuropathy
KW  - complications
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Myotonic Dystrophy
KW  - Pedigree
KW  - Physical Examination
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1212/wnl.41.1.80
ER  -