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Journal of Neurogenetics
|
May 1, 1986
Linkage analysis in a family with dominantly inherited torsion dystonia: exclusion of the pro-opiomelanocortin and glutamic acid decarboxylase genes and other chromosomal regions using DNA polymorphisms
X O Breakefield, S B Bressman, P L Kramer, et al.
Genomics
|
December 1, 1992
The CEPH consortium linkage map of human chromosome 15q
A M Bowcock, R I Barnes, R L White, et al.
Advances in Neurology
|
September 29, 1998
Clinical-genetic spectrum of primary dystonia
S B Bressman, D de Leon, D Raymond, et al.
Nature Photonics
|
June 8, 2026
Strong ultrafast nonlinear optical response from megaelectronvolt electrons in semiconductors
D Jeong, T R Hopper, Y Kim, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 18, 2005
Genetic heterogeneity in rapid onset dystonia-parkinsonism: description of a new family
K Kabakci, K Isbruch, K Schilling, et al.
Annals of Neurology
|
November 1, 1994
Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation
S B Bressman, D de Leon, P L Kramer, et al.
Annals of Neurology
|
February 1, 1990
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34
P L Kramer, D de Leon, L Ozelius, et al.
American Journal of Human Genetics
|
September 1, 1994
The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-Jews
P L Kramer, G A Heiman, T Gasser, et al.
Neurology
|
June 1, 1997
Secondary dystonia and the DYTI gene
S B Bressman, D de Leon, D Raymond, et al.
Molecular Biology & Medicine
|
December 1, 1986
DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomia
X O Breakefield, L Ozelius, M A Bothwell, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 49) with videos related to
Sort By:
Page
of 5
Journal of Neurogenetics
|
May 1, 1986
Linkage analysis in a family with dominantly inherited torsion dystonia: exclusion of the pro-opiomelanocortin and glutamic acid decarboxylase genes and other chromosomal regions using DNA polymorphisms
X O Breakefield, S B Bressman, P L Kramer, et al.
Genomics
|
December 1, 1992
The CEPH consortium linkage map of human chromosome 15q
A M Bowcock, R I Barnes, R L White, et al.
Advances in Neurology
|
September 29, 1998
Clinical-genetic spectrum of primary dystonia
S B Bressman, D de Leon, D Raymond, et al.
Nature Photonics
|
June 8, 2026
Strong ultrafast nonlinear optical response from megaelectronvolt electrons in semiconductors
D Jeong, T R Hopper, Y Kim, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 18, 2005
Genetic heterogeneity in rapid onset dystonia-parkinsonism: description of a new family
K Kabakci, K Isbruch, K Schilling, et al.
Annals of Neurology
|
November 1, 1994
Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation
S B Bressman, D de Leon, P L Kramer, et al.
Annals of Neurology
|
February 1, 1990
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34
P L Kramer, D de Leon, L Ozelius, et al.
American Journal of Human Genetics
|
September 1, 1994
The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-Jews
P L Kramer, G A Heiman, T Gasser, et al.
Neurology
|
June 1, 1997
Secondary dystonia and the DYTI gene
S B Bressman, D de Leon, D Raymond, et al.
Molecular Biology & Medicine
|
December 1, 1986
DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomia
X O Breakefield, L Ozelius, M A Bothwell, et al.
Page
of 5