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P M Green

Showing results (61-70 of 86) with videos related to

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Lancet (London, England)|March 16, 1991
Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII geneJ A Naylor, P M Green, A J Montandon, et al.
Genomics|July 1, 1992
Detection of point mutations and a gross deletion in six Hunter syndrome patientsR H Flomen, P M Green, D R Bentley, et al.
British Journal of Haematology|July 1, 1997
Further evidence for the importance of an androgen response element in the factor IX promoterG E Morgan, G Rowley, P M Green, et al.
British Journal of Haematology|December 22, 1999
Creation of a novel donor splice site in intron 1 of the factor VIII gene leads to activation of a 191 bp cryptic exon in two haemophilia A patientsR D Bagnall, N H Waseem, P M Green, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Analysis of the haemophilia A mutation in sporadic patients registered at the Royal London Hospital and their familiesL Tagliavacca, G Rowley, P M Green, et al.
FEBS Letters|August 22, 2001
Structural elements of the osteopontin SVVYGLR motif important for the interaction with alpha(4) integrinsP M Green, S B Ludbrook, D D Miller, et al.
Nucleic Acids Research|June 11, 1990
The incidence and distribution of CpG----TpG transitions in the coagulation factor IX gene. A fresh look at CpG mutational hotspotsP M Green, A J Montandon, D R Bentley, et al.
Current Studies in Hematology and Blood Transfusion|January 1, 1991
A new strategy for carrier and prenatal diagnosis and molecular studies in haemophilia BA J Montandon, P M Green, D R Bentley, et al.
Human Genetics|July 1, 1990
Two factor IX mutations in the family of an isolated haemophilia B patient: direct carrier diagnosis by amplification mismatch detection (AMD)A J Montandon, P M Green, D R Bentley, et al.
British Journal of Haematology|July 1, 1991
Haemophilia B mutations in a complete Swedish population sample: a test of new strategy for the genetic counselling of diseases with high mutational heterogeneityP M Green, A J Montandon, R Ljung, et al.
Pageof 9

Showing results (61-70 of 86) with videos related to

Sort By:
Pageof 9
Lancet (London, England)|March 16, 1991
Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII geneJ A Naylor, P M Green, A J Montandon, et al.
Genomics|July 1, 1992
Detection of point mutations and a gross deletion in six Hunter syndrome patientsR H Flomen, P M Green, D R Bentley, et al.
British Journal of Haematology|July 1, 1997
Further evidence for the importance of an androgen response element in the factor IX promoterG E Morgan, G Rowley, P M Green, et al.
British Journal of Haematology|December 22, 1999
Creation of a novel donor splice site in intron 1 of the factor VIII gene leads to activation of a 191 bp cryptic exon in two haemophilia A patientsR D Bagnall, N H Waseem, P M Green, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Analysis of the haemophilia A mutation in sporadic patients registered at the Royal London Hospital and their familiesL Tagliavacca, G Rowley, P M Green, et al.
FEBS Letters|August 22, 2001
Structural elements of the osteopontin SVVYGLR motif important for the interaction with alpha(4) integrinsP M Green, S B Ludbrook, D D Miller, et al.
Nucleic Acids Research|June 11, 1990
The incidence and distribution of CpG----TpG transitions in the coagulation factor IX gene. A fresh look at CpG mutational hotspotsP M Green, A J Montandon, D R Bentley, et al.
Current Studies in Hematology and Blood Transfusion|January 1, 1991
A new strategy for carrier and prenatal diagnosis and molecular studies in haemophilia BA J Montandon, P M Green, D R Bentley, et al.
Human Genetics|July 1, 1990
Two factor IX mutations in the family of an isolated haemophilia B patient: direct carrier diagnosis by amplification mismatch detection (AMD)A J Montandon, P M Green, D R Bentley, et al.
British Journal of Haematology|July 1, 1991
Haemophilia B mutations in a complete Swedish population sample: a test of new strategy for the genetic counselling of diseases with high mutational heterogeneityP M Green, A J Montandon, R Ljung, et al.
Pageof 9