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Current Opinion in Neurology
|
April 29, 1998
Craniofacial developmental abnormalities
F V Elmslie, W Reardon
Journal of the Royal Society of Medicine
|
May 1, 1996
Familial rectal pain: is it under-diagnosed?
F V Elmslie, J Wilson, M A Rossiter
Journal of Medical Genetics
|
April 1, 1995
Alagille syndrome: family studies
F V Elmslie, A J Vivian, H Gardiner, et al.
Journal of Medical Genetics
|
May 1, 1996
Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis
F V Elmslie, S M Hutchings, V Spencer, et al.
American Journal of Human Genetics
|
September 1, 1996
Linkage analysis of juvenile myoclonic epilepsy and microsatellite loci spanning 61 cM of human chromosome 6p in 19 nuclear pedigrees provides no evidence for a susceptibility locus in this region
F V Elmslie, M P Williamson, M Rees, et al.
Acta Neurologica Scandinavica
|
July 1, 1997
Linkage analysis between idiopathic generalized epilepsies and the GABA(A) receptor alpha5, beta3 and gamma3 subunit gene cluster on chromosome 15
T Sander, R Kretz, M P Williamson, et al.
Human Molecular Genetics
|
August 1, 1997
Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q
F V Elmslie, M Rees, M P Williamson, et al.
Neurology
|
August 8, 2007
Paroxysmal extreme pain disorder (previously familial rectal pain syndrome)
C R Fertleman, C D Ferrie, J Aicardi, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Current Opinion in Neurology
|
April 29, 1998
Craniofacial developmental abnormalities
F V Elmslie, W Reardon
Journal of the Royal Society of Medicine
|
May 1, 1996
Familial rectal pain: is it under-diagnosed?
F V Elmslie, J Wilson, M A Rossiter
Journal of Medical Genetics
|
April 1, 1995
Alagille syndrome: family studies
F V Elmslie, A J Vivian, H Gardiner, et al.
Journal of Medical Genetics
|
May 1, 1996
Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis
F V Elmslie, S M Hutchings, V Spencer, et al.
American Journal of Human Genetics
|
September 1, 1996
Linkage analysis of juvenile myoclonic epilepsy and microsatellite loci spanning 61 cM of human chromosome 6p in 19 nuclear pedigrees provides no evidence for a susceptibility locus in this region
F V Elmslie, M P Williamson, M Rees, et al.
Acta Neurologica Scandinavica
|
July 1, 1997
Linkage analysis between idiopathic generalized epilepsies and the GABA(A) receptor alpha5, beta3 and gamma3 subunit gene cluster on chromosome 15
T Sander, R Kretz, M P Williamson, et al.
Human Molecular Genetics
|
August 1, 1997
Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q
F V Elmslie, M Rees, M P Williamson, et al.
Neurology
|
August 8, 2007
Paroxysmal extreme pain disorder (previously familial rectal pain syndrome)
C R Fertleman, C D Ferrie, J Aicardi, et al.
Page
of 1