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Lancet (London, England)
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January 15, 1983
Cellular hypersensitivity to UV-A: a clue to the aetiology of actinic reticuloid?
F Giannelli, P K Botcherby, B Marimo, et al.
Methods in Molecular Medicine
|
February 23, 2011
Detection of mutations in hemophilia a patients by chemical cleavage of mismatch method
N H Waseem, R Bagnall, P M Green, et al.
Thrombosis and Haemostasis
|
July 15, 1999
Start of UK confidential haemophilia A database: analysis of 142 patients by solid phase fluorescent chemical cleavage of mismatch. Haemophilia Centres
N H Waseem, R Bagnall, P M Green, et al.
Genomics
|
February 1, 1993
Vertical integration of cosmid and YAC resources for interval mapping on the X-chromosome
J Holland, A J Coffey, F Giannelli, et al.
Thrombosis and Haemostasis
|
May 1, 1994
First report on UK database of haemophilia B mutations and pedigrees. UK Haemophilia Centres
S Saad, G Rowley, L Tagliavacca, et al.
Molecular Biology & Medicine
|
April 1, 1988
Partial deletion by illegitimate recombination of the factor IX gene in a haemophilia B family with two inhibitor patients
P M Green, D R Bentley, R S Mibashan, et al.
Human Molecular Genetics
|
January 1, 1993
Analysis of factor VIII mRNA reveals defects in everyone of 28 haemophilia A patients
J A Naylor, P M Green, C R Rizza, et al.
Prenatal Diagnosis
|
May 1, 1984
Mitomycin C induced chromosome damage in fetal blood cultures and prenatal diagnosis of Fanconi's anaemia
J Shipley, C H Rodeck, C Garrett, et al.
Nucleic Acids Research
|
May 11, 1989
Direct detection of point mutations by mismatch analysis: application to haemophilia B
A J Montandon, P M Green, F Giannelli, et al.
British Journal of Haematology
|
August 12, 2008
Haemophilia A mutations in the UK: results of screening one-third of the population
P M Green, R D Bagnall, N H Waseem, et al.
Page
of 10
Search research articles
Search
Showing results (21-30 of 97) with videos related to
Sort By:
Page
of 10
Lancet (London, England)
|
January 15, 1983
Cellular hypersensitivity to UV-A: a clue to the aetiology of actinic reticuloid?
F Giannelli, P K Botcherby, B Marimo, et al.
Methods in Molecular Medicine
|
February 23, 2011
Detection of mutations in hemophilia a patients by chemical cleavage of mismatch method
N H Waseem, R Bagnall, P M Green, et al.
Thrombosis and Haemostasis
|
July 15, 1999
Start of UK confidential haemophilia A database: analysis of 142 patients by solid phase fluorescent chemical cleavage of mismatch. Haemophilia Centres
N H Waseem, R Bagnall, P M Green, et al.
Genomics
|
February 1, 1993
Vertical integration of cosmid and YAC resources for interval mapping on the X-chromosome
J Holland, A J Coffey, F Giannelli, et al.
Thrombosis and Haemostasis
|
May 1, 1994
First report on UK database of haemophilia B mutations and pedigrees. UK Haemophilia Centres
S Saad, G Rowley, L Tagliavacca, et al.
Molecular Biology & Medicine
|
April 1, 1988
Partial deletion by illegitimate recombination of the factor IX gene in a haemophilia B family with two inhibitor patients
P M Green, D R Bentley, R S Mibashan, et al.
Human Molecular Genetics
|
January 1, 1993
Analysis of factor VIII mRNA reveals defects in everyone of 28 haemophilia A patients
J A Naylor, P M Green, C R Rizza, et al.
Prenatal Diagnosis
|
May 1, 1984
Mitomycin C induced chromosome damage in fetal blood cultures and prenatal diagnosis of Fanconi's anaemia
J Shipley, C H Rodeck, C Garrett, et al.
Nucleic Acids Research
|
May 11, 1989
Direct detection of point mutations by mismatch analysis: application to haemophilia B
A J Montandon, P M Green, F Giannelli, et al.
British Journal of Haematology
|
August 12, 2008
Haemophilia A mutations in the UK: results of screening one-third of the population
P M Green, R D Bagnall, N H Waseem, et al.
Page
of 10