Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P M Green

Showing results (51-60 of 86) with videos related to

Pageof 9
Sort By:
Human Mutation|January 1, 1993
Haemophilia B caused by a missense mutation in the prepeptide sequence of factor IXP M Green, V E Mitchell, A McGraw, et al.
Molecular Microbiology|June 11, 1998
Sequence, exon-intron organization, transcription and mutational analysis of prnA, the gene encoding the transcriptional activator of the prn gene cluster in Aspergillus nidulansB Cazelle, A Pokorska, E Hull, et al.
Journal of Thrombosis and Haemostasis : JTH|December 17, 2003
DNA variation in a 13-Mb region including the F9 gene: inferring the genealogical history and causal role of a hemophilia B mutation (IVS 5+13 A-->G)T Anagnostopoulos, A P Morris, K L Ayres, et al.
Journal of Medical Genetics|April 25, 2000
Somatic mosaicism associated with a mild Alport syndrome phenotypeK E Plant, E Boye, P M Green, 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 modelF Giannelli, S Saad, A J Montandon, et al.
Thrombosis and Haemostasis|January 23, 1992
Haplotype analysis of identical factor IX mutants using PCRP M Green, A J Montandon, R Ljung, et al.
The EMBO Journal|April 1, 1989
Molecular pathology of haemophilia BP M Green, D R Bentley, R S Mibashan, et al.
Human Molecular Genetics|January 1, 1993
Determination of the organisation of coding sequences within the iduronate sulphate sulphatase (IDS) geneR H Flomen, E P Green, P M Green, et al.
Journal of Medical Genetics|August 1, 1992
Beta-hexosaminidase splice site mutation has a high frequency among non-Jewish Tay-Sachs disease carriers from the British IslesE C Landels, P M Green, I H Ellis, et al.
Journal of Medical Genetics|March 1, 1991
Frequency of the Tay-Sachs disease splice and insertion mutations in the UK Ashkenazi Jewish populationE C Landels, I H Ellis, A H Fensom, et al.
Pageof 9

Showing results (51-60 of 86) with videos related to

Sort By:
Pageof 9
Human Mutation|January 1, 1993
Haemophilia B caused by a missense mutation in the prepeptide sequence of factor IXP M Green, V E Mitchell, A McGraw, et al.
Molecular Microbiology|June 11, 1998
Sequence, exon-intron organization, transcription and mutational analysis of prnA, the gene encoding the transcriptional activator of the prn gene cluster in Aspergillus nidulansB Cazelle, A Pokorska, E Hull, et al.
Journal of Thrombosis and Haemostasis : JTH|December 17, 2003
DNA variation in a 13-Mb region including the F9 gene: inferring the genealogical history and causal role of a hemophilia B mutation (IVS 5+13 A-->G)T Anagnostopoulos, A P Morris, K L Ayres, et al.
Journal of Medical Genetics|April 25, 2000
Somatic mosaicism associated with a mild Alport syndrome phenotypeK E Plant, E Boye, P M Green, 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 modelF Giannelli, S Saad, A J Montandon, et al.
Thrombosis and Haemostasis|January 23, 1992
Haplotype analysis of identical factor IX mutants using PCRP M Green, A J Montandon, R Ljung, et al.
The EMBO Journal|April 1, 1989
Molecular pathology of haemophilia BP M Green, D R Bentley, R S Mibashan, et al.
Human Molecular Genetics|January 1, 1993
Determination of the organisation of coding sequences within the iduronate sulphate sulphatase (IDS) geneR H Flomen, E P Green, P M Green, et al.
Journal of Medical Genetics|August 1, 1992
Beta-hexosaminidase splice site mutation has a high frequency among non-Jewish Tay-Sachs disease carriers from the British IslesE C Landels, P M Green, I H Ellis, et al.
Journal of Medical Genetics|March 1, 1991
Frequency of the Tay-Sachs disease splice and insertion mutations in the UK Ashkenazi Jewish populationE C Landels, I H Ellis, A H Fensom, et al.
Pageof 9