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American Journal of Human Genetics|December 1, 1999
Mutation rates in humans. I. Overall and sex-specific rates obtained from a population study of hemophilia BP M Green, S Saad, C M Lewis, et al.Methods in Molecular Medicine|February 23, 2011
Detection of mutations in hemophilia a patients by chemical cleavage of mismatch methodN 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 CentresN 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-chromosomeJ 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 CentresS 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 patientsP 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 patientsJ 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 anaemiaJ 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 BA 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 populationP M Green, R D Bagnall, N H Waseem, et al.Pageof 10