Search research articles
Contact Us
Filters
Showing results (51-60 of 140) with videos related to
Page
of 14
Sort By:
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.
Radiation Research
|
October 1, 1981
Xeroderma Pigmentosum and medulloblastoma: chromosomal damage to lymphocytes during radiotherapy
F Giannelli, J Avery, P E Polani, et al.
The Journal of Investigative Dermatology
|
April 1, 1978
A human subject with a new defect in repair of ultraviolet damage
C F Arlett, A R Lehmann, F Giannelli, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
August 1, 1991
Genetics and molecular biology of haemophilias A and B
P M Green, A J Montandon, D R Bentley, et al.
PCR Methods and Applications
|
April 1, 1994
Mutation detection by fluorescent chemical cleavage: application to hemophilia B
I I Haris, P M Green, D R Bentley, et al.
Page
of 14
Search research articles
Search
Showing results (51-60 of 140) with videos related to
Sort By:
Page
of 14
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.
Radiation Research
|
October 1, 1981
Xeroderma Pigmentosum and medulloblastoma: chromosomal damage to lymphocytes during radiotherapy
F Giannelli, J Avery, P E Polani, et al.
The Journal of Investigative Dermatology
|
April 1, 1978
A human subject with a new defect in repair of ultraviolet damage
C F Arlett, A R Lehmann, F Giannelli, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
August 1, 1991
Genetics and molecular biology of haemophilias A and B
P M Green, A J Montandon, D R Bentley, et al.
PCR Methods and Applications
|
April 1, 1994
Mutation detection by fluorescent chemical cleavage: application to hemophilia B
I I Haris, P M Green, D R Bentley, et al.
Page
of 14