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Trends in Genetics : TIG
|
November 20, 1998
Coordination of human genome sequencing via a consensus framework map
D R Bentley, K D Pruitt, P Deloukas, et al.
Journal of Medical Genetics
|
September 1, 1992
A new strategy for the genetic counselling of diseases of marked mutational heterogeneity: haemophilia B as a model
F Giannelli, S Saad, A J Montandon, et al.
American Journal of Human Genetics
|
August 1, 1991
Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytes
R G Roberts, T F Barby, E Manners, et al.
The EMBO Journal
|
April 1, 1989
Molecular pathology of haemophilia B
P M Green, D R Bentley, R S Mibashan, et al.
Nucleic Acids Research
|
October 25, 1991
A MseI polymorphism in exon 48 of the dystrophin gene
S C Yau, R G Roberts, D R Bentley, et al.
Human Molecular Genetics
|
January 1, 1993
Determination of the organisation of coding sequences within the iduronate sulphate sulphatase (IDS) gene
R H Flomen, E P Green, P M Green, et al.
Nucleic Acids Research
|
January 25, 1989
Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy
R G Roberts, C G Cole, K A Hart, et al.
Genomics
|
July 1, 1992
Detection of point mutations and a gross deletion in six Hunter syndrome patients
R H Flomen, P M Green, D R Bentley, et al.
The Journal of Experimental Medicine
|
June 1, 1992
A variable number of tandem repeats locus within the human complement C2 gene is associated with a retroposon derived from a human endogenous retrovirus
Z B Zhu, S L Hsieh, D R Bentley, et al.
Genomics
|
December 1, 1992
Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplification
C G Cole, K Patel, J Shipley, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 88) with videos related to
Sort By:
Page
of 9
Trends in Genetics : TIG
|
November 20, 1998
Coordination of human genome sequencing via a consensus framework map
D R Bentley, K D Pruitt, P Deloukas, et al.
Journal of Medical Genetics
|
September 1, 1992
A new strategy for the genetic counselling of diseases of marked mutational heterogeneity: haemophilia B as a model
F Giannelli, S Saad, A J Montandon, et al.
American Journal of Human Genetics
|
August 1, 1991
Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytes
R G Roberts, T F Barby, E Manners, et al.
The EMBO Journal
|
April 1, 1989
Molecular pathology of haemophilia B
P M Green, D R Bentley, R S Mibashan, et al.
Nucleic Acids Research
|
October 25, 1991
A MseI polymorphism in exon 48 of the dystrophin gene
S C Yau, R G Roberts, D R Bentley, et al.
Human Molecular Genetics
|
January 1, 1993
Determination of the organisation of coding sequences within the iduronate sulphate sulphatase (IDS) gene
R H Flomen, E P Green, P M Green, et al.
Nucleic Acids Research
|
January 25, 1989
Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy
R G Roberts, C G Cole, K A Hart, et al.
Genomics
|
July 1, 1992
Detection of point mutations and a gross deletion in six Hunter syndrome patients
R H Flomen, P M Green, D R Bentley, et al.
The Journal of Experimental Medicine
|
June 1, 1992
A variable number of tandem repeats locus within the human complement C2 gene is associated with a retroposon derived from a human endogenous retrovirus
Z B Zhu, S L Hsieh, D R Bentley, et al.
Genomics
|
December 1, 1992
Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplification
C G Cole, K Patel, J Shipley, et al.
Page
of 9