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Acta Paediatrica (Oslo, Norway : 1992)
|
January 29, 2010
13q33.2 deletion: a rare cause of ambiguous genitalia in a male newborn with growth restriction
J H Andresen, S Aftimos, E Doherty, et al.
Journal of Medical Genetics
|
March 8, 2003
Paternal uniparental disomy in monozygotic twins discordant for hemihypertrophy
P M H West, D R Love, P M Stapleton, et al.
Acta Physiologica (Oxford, England)
|
March 25, 2010
Zebrafish as a model for long QT syndrome: the evidence and the means of manipulating zebrafish gene expression
I U S Leong, J R Skinner, A N Shelling, et al.
Acta Anaesthesiologica Scandinavica
|
May 30, 1998
Influence of premedication with diazepam or morphine on the induction dose of eltanolone
A Czuchwicki, J L Plummer, D R Love, et al.
Nucleic Acids Research
|
August 11, 1991
A new DNA marker, D6S129, identifies a HindIII polymorphism on chromosome 6q
B C Byth, D R Love, M R Passos-Bueno, et al.
Molecular and Cellular Probes
|
August 11, 1999
Comparative semi-automated analysis of (CAG) repeats in the Huntington disease gene: use of internal standards
L C Williams, M R Hegde, G Herrera, et al.
Applied and Environmental Microbiology
|
March 1, 1991
Cloning, sequence analysis, and expression in Escherichia coli of a gene coding for a beta-mannanase from the extremely thermophilic bacterium "Caldocellum saccharolyticum"
E Lüthi, N B Jasmat, R A Grayling, et al.
Genetic Testing
|
September 12, 2001
Compound heterozygosity at the FMR1 gene
M R Hegde, M Fawkner, B Chong, et al.
Human Mutation
|
January 1, 1997
Mutations in the adrenoleukodystrophy gene
A Dodd, S A Rowland, S L Hawkes, et al.
Neuromuscular Disorders : NMD
|
January 1, 1993
Dystrophin and dystrophin-related proteins: a review of protein and RNA studies
D R Love, B C Byth, J M Tinsley, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 85) with videos related to
Sort By:
Page
of 9
Acta Paediatrica (Oslo, Norway : 1992)
|
January 29, 2010
13q33.2 deletion: a rare cause of ambiguous genitalia in a male newborn with growth restriction
J H Andresen, S Aftimos, E Doherty, et al.
Journal of Medical Genetics
|
March 8, 2003
Paternal uniparental disomy in monozygotic twins discordant for hemihypertrophy
P M H West, D R Love, P M Stapleton, et al.
Acta Physiologica (Oxford, England)
|
March 25, 2010
Zebrafish as a model for long QT syndrome: the evidence and the means of manipulating zebrafish gene expression
I U S Leong, J R Skinner, A N Shelling, et al.
Acta Anaesthesiologica Scandinavica
|
May 30, 1998
Influence of premedication with diazepam or morphine on the induction dose of eltanolone
A Czuchwicki, J L Plummer, D R Love, et al.
Nucleic Acids Research
|
August 11, 1991
A new DNA marker, D6S129, identifies a HindIII polymorphism on chromosome 6q
B C Byth, D R Love, M R Passos-Bueno, et al.
Molecular and Cellular Probes
|
August 11, 1999
Comparative semi-automated analysis of (CAG) repeats in the Huntington disease gene: use of internal standards
L C Williams, M R Hegde, G Herrera, et al.
Applied and Environmental Microbiology
|
March 1, 1991
Cloning, sequence analysis, and expression in Escherichia coli of a gene coding for a beta-mannanase from the extremely thermophilic bacterium "Caldocellum saccharolyticum"
E Lüthi, N B Jasmat, R A Grayling, et al.
Genetic Testing
|
September 12, 2001
Compound heterozygosity at the FMR1 gene
M R Hegde, M Fawkner, B Chong, et al.
Human Mutation
|
January 1, 1997
Mutations in the adrenoleukodystrophy gene
A Dodd, S A Rowland, S L Hawkes, et al.
Neuromuscular Disorders : NMD
|
January 1, 1993
Dystrophin and dystrophin-related proteins: a review of protein and RNA studies
D R Love, B C Byth, J M Tinsley, et al.
Page
of 9