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Human Molecular Genetics
|
April 1, 1995
Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy
N R Rodrigues, N Owen, K Talbot, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 3, 2004
De novo paracentric inversion 14q13q24.1 in a patient with severe involuntary movements, epilepsy, oligodontia and dysmorphic features
M Peippo, C Tengström, M Arvio, et al.
Alcohol and Alcoholism (Oxford, Oxfordshire). Supplement
|
January 1, 1987
Ethanol-induced modulation of hippocampal EEG and cerebral 2-deoxyglucose accumulation in rat lines with differing alcohol sensitivities
E R Korpi, F Lindroos, I Pyykkö, et al.
Cell Adhesion and Communication
|
September 1, 1996
Heterologous expression of alpha 1-integrin cDNA generates variable ligand specificities and alterations in cell shape
L D Wong, A B Sondheim, K R Zachow, et al.
Genomics
|
July 1, 1993
A fourth example suggests that premature termination codons in the COL2A1 gene are a common cause of the Stickler syndrome: analysis of the COL2A1 gene by denaturing gradient gel electrophoresis
P Ritvaniemi, J Hyland, J Ignatius, et al.
Neuropediatrics
|
May 1, 1987
Visual evoked potentials in high-risk infants
V K Häkkinen, J Ignatius, M Koskinen, et al.
The Journal of Laboratory and Clinical Medicine
|
January 11, 2000
Smith-Lemli-Opitz syndrome and other sterol disorders among Finns with developmental disabilities
M J Nissinen, H Gylling, M Kaski, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 1, 1990
Neuron-specific expression of high-molecular-weight clathrin light chain
D H Wong, M J Ignatius, G Parosky, et al.
Journal of Biomedical Materials Research
|
April 29, 1998
Bioactive surface coatings for nanoscale instruments: effects on CNS neurons
M J Ignatius, N Sawhney, A Gupta, et al.
Human Molecular Genetics
|
December 26, 2001
Dissecting a population genome for targeted screening of disease mutations
T Pastinen, M Perola, J Ignatius, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 91) with videos related to
Sort By:
Page
of 10
Human Molecular Genetics
|
April 1, 1995
Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy
N R Rodrigues, N Owen, K Talbot, et al.
Genetic Counseling (Geneva, Switzerland)
|
November 3, 2004
De novo paracentric inversion 14q13q24.1 in a patient with severe involuntary movements, epilepsy, oligodontia and dysmorphic features
M Peippo, C Tengström, M Arvio, et al.
Alcohol and Alcoholism (Oxford, Oxfordshire). Supplement
|
January 1, 1987
Ethanol-induced modulation of hippocampal EEG and cerebral 2-deoxyglucose accumulation in rat lines with differing alcohol sensitivities
E R Korpi, F Lindroos, I Pyykkö, et al.
Cell Adhesion and Communication
|
September 1, 1996
Heterologous expression of alpha 1-integrin cDNA generates variable ligand specificities and alterations in cell shape
L D Wong, A B Sondheim, K R Zachow, et al.
Genomics
|
July 1, 1993
A fourth example suggests that premature termination codons in the COL2A1 gene are a common cause of the Stickler syndrome: analysis of the COL2A1 gene by denaturing gradient gel electrophoresis
P Ritvaniemi, J Hyland, J Ignatius, et al.
Neuropediatrics
|
May 1, 1987
Visual evoked potentials in high-risk infants
V K Häkkinen, J Ignatius, M Koskinen, et al.
The Journal of Laboratory and Clinical Medicine
|
January 11, 2000
Smith-Lemli-Opitz syndrome and other sterol disorders among Finns with developmental disabilities
M J Nissinen, H Gylling, M Kaski, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 1, 1990
Neuron-specific expression of high-molecular-weight clathrin light chain
D H Wong, M J Ignatius, G Parosky, et al.
Journal of Biomedical Materials Research
|
April 29, 1998
Bioactive surface coatings for nanoscale instruments: effects on CNS neurons
M J Ignatius, N Sawhney, A Gupta, et al.
Human Molecular Genetics
|
December 26, 2001
Dissecting a population genome for targeted screening of disease mutations
T Pastinen, M Perola, J Ignatius, et al.
Page
of 10