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J Ignatius

Showing results (31-40 of 91) with videos related to

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The American Journal of Dermatopathology|June 1, 1993
Recessive ichthyosis congenita type IVK M Niemi, K Kuokkanen, L Kanerva, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 1, 1985
Association of nerve growth factor receptors with the triton X-100 cytoskeleton of PC12 cellsR D Vale, M J Ignatius, E M Shooter
American Journal of Human Genetics|July 1, 1997
Genomic variation and gene conversion in spinal muscular atrophy: implications for disease process and clinical phenotypeL Campbell, A Potter, J Ignatius, et al.
Human Genetics|May 1, 1992
Huntington disease in Finland: a molecular and genealogical studyE Ikonen, J Ignatius, R Norio, et al.
Archives of Dermatological Research|January 1, 1992
Clinical, light and electron microscopic features of recessive ichthyosis congenita type IIIK M Niemi, L Kanerva, C F Wahlgren, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1997
[CATCH-22: a microdeletion of chromosome 22 behind the polymorphous syndrome]M Somer, J Ignatius, P Vehmanen, et al.
Journal of Medical Genetics|September 1, 1995
Clinical features of nine males with molecularly defined deletions of the Y chromosome long armP Salo, J Ignatius, K O Simola, et al.
Pharmacology, Biochemistry, and Behavior|May 1, 1988
Hippocampal rhythmic slow activity in rat lines selected for differences in ethanol-induced motor impairmentP Kaheinen, E R Korpi, I Pyykkö, et al.
Journal of Medical Genetics|June 1, 1996
Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3J Ignatius, S Knuutila, S W Scherer, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotypeK Talbot, N R Rodrigues, J Ignatius, et al.
Pageof 10

Showing results (31-40 of 91) with videos related to

Sort By:
Pageof 10
The American Journal of Dermatopathology|June 1, 1993
Recessive ichthyosis congenita type IVK M Niemi, K Kuokkanen, L Kanerva, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 1, 1985
Association of nerve growth factor receptors with the triton X-100 cytoskeleton of PC12 cellsR D Vale, M J Ignatius, E M Shooter
American Journal of Human Genetics|July 1, 1997
Genomic variation and gene conversion in spinal muscular atrophy: implications for disease process and clinical phenotypeL Campbell, A Potter, J Ignatius, et al.
Human Genetics|May 1, 1992
Huntington disease in Finland: a molecular and genealogical studyE Ikonen, J Ignatius, R Norio, et al.
Archives of Dermatological Research|January 1, 1992
Clinical, light and electron microscopic features of recessive ichthyosis congenita type IIIK M Niemi, L Kanerva, C F Wahlgren, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1997
[CATCH-22: a microdeletion of chromosome 22 behind the polymorphous syndrome]M Somer, J Ignatius, P Vehmanen, et al.
Journal of Medical Genetics|September 1, 1995
Clinical features of nine males with molecularly defined deletions of the Y chromosome long armP Salo, J Ignatius, K O Simola, et al.
Pharmacology, Biochemistry, and Behavior|May 1, 1988
Hippocampal rhythmic slow activity in rat lines selected for differences in ethanol-induced motor impairmentP Kaheinen, E R Korpi, I Pyykkö, et al.
Journal of Medical Genetics|June 1, 1996
Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3J Ignatius, S Knuutila, S W Scherer, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotypeK Talbot, N R Rodrigues, J Ignatius, et al.
Pageof 10