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Computer Methods and Programs in Biomedicine
|
January 1, 1995
Development of a directory of genetic probes as a shared institutional resource
G A Orr, P K Rogan
Human Mutation
|
January 1, 1995
Using information content and base frequencies to distinguish mutations from genetic polymorphisms in splice junction recognition sites
P K Rogan, T D Schneider
Applied and Theoretical Electrophoresis : the Official Journal of the International Electrophoresis Society
|
January 1, 1991
Automatic detection of noisy spots in two-dimensional Southern blots. International Electrophoresis Society Meeting, Washington DC, March 16-19, 1991
P F Lemkin, P K Rogan
Nucleic Acids Research
|
April 11, 1986
Conservation in the 5' region of the long interspersed mouse L1 repeat: implications of comparative sequence analysis
E Mottez, P K Rogan, L Manuelidis
Molecular Biology and Evolution
|
July 1, 1987
L1 repeat elements in the human epsilon-G gamma-globin gene intergenic region: sequence analysis and concerted evolution within this family
P K Rogan, J Pan, S M Weissman
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
April 29, 2006
Predicting severity of haemophilia A and B splicing mutations by information analysis
Y von Kodolitsch, J Berger, P K Rogan
Human Genetics
|
April 1, 1998
Transmission of mitochondrial DNA heteroplasmy in normal pedigrees
C D Gocke, F A Benko, P K Rogan
Journal of Medical Genetics
|
August 28, 1999
Maternal uniparental disomy of chromosome 14 confined to an interstitial segment (14q23-14q24.2)
R A Martin, D W Sabol, P K Rogan
American Journal of Medical Genetics
|
March 17, 1999
Maternal uniparental disomy of chromosome 21 in a normal child
P K Rogan, D W Sabol, H H Punnett
Genome Research
|
May 31, 2001
Sequence-based design of single-copy genomic DNA probes for fluorescence in situ hybridization
P K Rogan, P M Cazcarro, J H Knoll
Page
of 5
Search research articles
Search
Showing results (1-10 of 45) with videos related to
Sort By:
Page
of 5
Computer Methods and Programs in Biomedicine
|
January 1, 1995
Development of a directory of genetic probes as a shared institutional resource
G A Orr, P K Rogan
Human Mutation
|
January 1, 1995
Using information content and base frequencies to distinguish mutations from genetic polymorphisms in splice junction recognition sites
P K Rogan, T D Schneider
Applied and Theoretical Electrophoresis : the Official Journal of the International Electrophoresis Society
|
January 1, 1991
Automatic detection of noisy spots in two-dimensional Southern blots. International Electrophoresis Society Meeting, Washington DC, March 16-19, 1991
P F Lemkin, P K Rogan
Nucleic Acids Research
|
April 11, 1986
Conservation in the 5' region of the long interspersed mouse L1 repeat: implications of comparative sequence analysis
E Mottez, P K Rogan, L Manuelidis
Molecular Biology and Evolution
|
July 1, 1987
L1 repeat elements in the human epsilon-G gamma-globin gene intergenic region: sequence analysis and concerted evolution within this family
P K Rogan, J Pan, S M Weissman
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
April 29, 2006
Predicting severity of haemophilia A and B splicing mutations by information analysis
Y von Kodolitsch, J Berger, P K Rogan
Human Genetics
|
April 1, 1998
Transmission of mitochondrial DNA heteroplasmy in normal pedigrees
C D Gocke, F A Benko, P K Rogan
Journal of Medical Genetics
|
August 28, 1999
Maternal uniparental disomy of chromosome 14 confined to an interstitial segment (14q23-14q24.2)
R A Martin, D W Sabol, P K Rogan
American Journal of Medical Genetics
|
March 17, 1999
Maternal uniparental disomy of chromosome 21 in a normal child
P K Rogan, D W Sabol, H H Punnett
Genome Research
|
May 31, 2001
Sequence-based design of single-copy genomic DNA probes for fluorescence in situ hybridization
P K Rogan, P M Cazcarro, J H Knoll
Page
of 5