Search research articles
Contact Us
Filters
Showing results (1-10 of 68) with videos related to
Page
of 7
Sort By:
Human Genetics
|
August 1, 1997
Towards a unified nomenclature describing voltage-gated calcium channel genes
P Lory, R A Ophoff, J Nahmias
Human Molecular Genetics
|
February 22, 2001
The genome-wide distribution of background linkage disequilibrium in a population isolate
S K Service, R A Ophoff, N B Freimer
Oncogene
|
May 1, 1994
Kras-2 alleles, mutations, and lung tumor susceptibility in the mouse--an evaluation
R J Fijneman, R A Ophoff, A A Hart, et al.
Trends in Pharmacological Sciences
|
June 5, 1998
P/Q-type Ca2+ channel defects in migraine, ataxia and epilepsy
R A Ophoff, G M Terwindt, R R Frants, et al.
Histology and Histopathology
|
August 5, 1998
Genetics and pathology of voltage-gated Ca2+ channels
R A Ophoff, G M Terwindt, M D Ferrari, et al.
Cytogenetic and Genome Research
|
November 8, 2011
Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research
R Hochstenbach, J E Buizer-Voskamp, J A S Vorstman, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
June 12, 1998
[Channelopathies: a genetic explanation of migraine and other paroxysmal neurologic disorders]
G M Terwindt, R A Ophoff, J Haan, et al.
Cephalalgia : an International Journal of Headache
|
May 1, 1996
Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG
G M Terwindt, R A Ophoff, J Haan, et al.
Current Opinion in Neurology
|
June 1, 1997
The quest for migraine genes
G M Terwindt, J Haan, R A Ophoff, et al.
Neurologia (Barcelona, Spain)
|
January 22, 1998
Familial hemiplegic migraine: involvement of a calcium neuronal channel
R A Ophoff, G M Terwindt, M N Vergouwe, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 68) with videos related to
Sort By:
Page
of 7
Human Genetics
|
August 1, 1997
Towards a unified nomenclature describing voltage-gated calcium channel genes
P Lory, R A Ophoff, J Nahmias
Human Molecular Genetics
|
February 22, 2001
The genome-wide distribution of background linkage disequilibrium in a population isolate
S K Service, R A Ophoff, N B Freimer
Oncogene
|
May 1, 1994
Kras-2 alleles, mutations, and lung tumor susceptibility in the mouse--an evaluation
R J Fijneman, R A Ophoff, A A Hart, et al.
Trends in Pharmacological Sciences
|
June 5, 1998
P/Q-type Ca2+ channel defects in migraine, ataxia and epilepsy
R A Ophoff, G M Terwindt, R R Frants, et al.
Histology and Histopathology
|
August 5, 1998
Genetics and pathology of voltage-gated Ca2+ channels
R A Ophoff, G M Terwindt, M D Ferrari, et al.
Cytogenetic and Genome Research
|
November 8, 2011
Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research
R Hochstenbach, J E Buizer-Voskamp, J A S Vorstman, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
June 12, 1998
[Channelopathies: a genetic explanation of migraine and other paroxysmal neurologic disorders]
G M Terwindt, R A Ophoff, J Haan, et al.
Cephalalgia : an International Journal of Headache
|
May 1, 1996
Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG
G M Terwindt, R A Ophoff, J Haan, et al.
Current Opinion in Neurology
|
June 1, 1997
The quest for migraine genes
G M Terwindt, J Haan, R A Ophoff, et al.
Neurologia (Barcelona, Spain)
|
January 22, 1998
Familial hemiplegic migraine: involvement of a calcium neuronal channel
R A Ophoff, G M Terwindt, M N Vergouwe, et al.
Page
of 7