P. Green

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Haemophilia B: database of point mutations and short additions and deletions.

P. Reitsma, K. High, R. Schwaab, 1990, Nucleic acids research.

Start of UK Confidential Haemophilia A Database: Analysis of 142 Patients by Solid Phase Fluorescent Chemical Cleavage of Mismatch

F. Giannelli, P. Green, N. Waseem, 1999, Thrombosis and Haemostasis.

Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII gene

P. Green, C. Rizza, F. Giannelli, 1991, The Lancet.

Polymorphism and hemophilia A causing inversions in distal Xq28: a complex picture

F. Giannelli, P. Green, R. Bagnall, 2005, Journal of thrombosis and haemostasis : JTH.

P. Green, F. Giannelli, P. Green, 2006, Journal of thrombosis and haemostasis : JTH.

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 patients

P. Green, B. Colvin, F. Giannelli, 1999, British journal of haematology.

The molecular basis of haemophilia A and B.

P. Green, F. Giannelli, P. Green, 1996, Bailliere's clinical haematology.

Mutation rates in humans. II. Sporadic mutation-specific rates and rate of detrimental human mutations inferred from hemophilia B.

F. Giannelli, P. Green, T. Anagnostopoulos, 1999, American journal of human genetics.

Detection of point mutations and a gross deletion in six Hunter syndrome patients.

D. Bentley, F. Giannelli, P. Green, 1992, Genomics.

Analysis of factor VIII mRNA reveals defects in everyone of 28 haemophilia A patients.

F. Giannelli, P. Green, J. Naylor, 1993, Human molecular genetics.

Direct detection of point mutations by mismatch analysis: application to haemophilia B.

D. Bentley, F. Giannelli, P. Green, 1989, Nucleic acids research.

Hemophilia B mutational analysis.

P. Green, 1999, Methods in molecular medicine.

Factor VIII gene explains all cases of haemophilia A

P. Green, C. Rizza, F. Giannelli, 1992, The Lancet.

Direct estimate of the haemophilia B (factor IX deficiency) mutation rate and of the ratio of the sex-specific mutation rates in Sweden

D. Bentley, R. Ljung, I. Nilsson, 1992, Human Genetics.

Haemophilia B: database of point mutations and short additions and deletions, fifth edition, 1994.

P. Reitsma, R. Schwaab, G. Brownlee, 1994, Nucleic acids research.

Antenatal diagnosis of haemophilia B by amplification and electrophoresis of an exon fragment with a short deletion

R. Ljung, F. Giannelli, P. Green, 1992, European journal of haematology.

Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversions.

P. Green, S. Hassock, F. Giannelli, 1993, Human molecular genetics.

Haemophilia B: database of point mutations and short additions and deletions, 7th edition

M. Goossens, P. M. Green, S. S. Sommer, 1990, Nucleic Acids Res..

Haemophilia B: database of point mutations and short additions and deletions--eighth edition

M. Goossens, F. Giannelli, P. M. Green, 1998, Nucleic Acids Res..

First Report on UK Database of Haemophilia B Mutations and Pedigrees

P. Green, S. Saad, F. Giannelli, 1994, Thrombosis and Haemostasis.

Mutation rates in humans. I. Overall and sex-specific rates obtained from a population study of hemophilia B.

C. Lewis, S. Saad, F. Giannelli, 1999, American journal of human genetics.

Molecular pathology of haemophilia B.

D. Bentley, P. Green, R. Mibashan, 1989, The EMBO journal.

Haemophilia B mutations in a complete Swedish population sample: a test of new strategy for the genetic counselling of diseases with high mutational heterogeneity

D. Bentley, P. Green, R. Ljung, 1991, British journal of haematology.

Haemophilia B (sixth edition): a database of point mutations and short additions and deletions

M. Goossens, F. Giannelli, P. M. Green, 1996, Nucleic Acids Res..

Haemophilia B: database of point mutations and short additions and deletions--second edition.

P. Reitsma, K. High, D. Lillicrap, 1991, Nucleic acids research.

Partial deletion by illegitimate recombination of the factor IX gene in a haemophilia B family with two inhibitor patients.

D. Bentley, R. Mibashan, F. Giannelli, 1988, Molecular biology & medicine.

Two chimaeric transcription units result from an inversion breaking intron 1 of the factor VIII gene and a region reportedly affected by reciprocal translocations in T-cell leukaemia.

P. Green, P. Giangrande, F. Giannelli, 1996, Human molecular genetics.

Genetics and molecular biology of haemophilias A and B.

D. Bentley, F. Giannelli, P. Green, 1991, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Haemophilia B caused by a missense mutation in the prepeptide sequence of factor IX

F. Giannelli, P. Green, V. Mitchell, 1993, Human mutation.

Investigation of the factor VIII intron 22 repeated region (int22h) and the associated inversion junctions.

D. Bentley, P. Green, D. Buck, 1995, Human molecular genetics.

Haemophilia B: database of point mutations and short additions and deletions--third edition, 1992.

P. Reitsma, K. High, D. Lillicrap, 1992, Nucleic acids research.

Haemophilia A mutations in the UK: results of screening one‐third of the population

P. Green, F. Giannelli, P. Green, 2008, British journal of haematology.

The incidence and distribution of CpG----TpG transitions in the coagulation factor IX gene. A fresh look at CpG mutational hotspots.

D. Bentley, P. Green, R. Ljung, 1990, Nucleic acids research.

Determination of the organisation of coding sequences within the iduronate sulphate sulphatase (IDS) gene.

D. Bentley, P. Green, F. Giannelli, 1993, Human molecular genetics.

DNA variation in a 5-Mb region of the X chromosome and estimates of sex-specific/type-specific mutation rates.

C. Lewis, F. Giannelli, P. Green, 1999, American journal of human genetics.

Characterization of the gene (VBP1) and transcript for the von Hippel-Lindau binding protein and isolation of the highly conserved murine homologue.

P. Green, F. Giannelli, P. Green, 1997, Genomics.

Unusual expression of the F9 gene in peripheral lymphocytes hinders investigation of F9 mRNA in hemophilia B patients

F. Giannelli, P. Green, G. Rowley, 2003, Journal of thrombosis and haemostasis : JTH.

Direct sequencing of PCR-amplified DNA.

F. Giannelli, P. Green, 1994, Molecular biotechnology.

Ultrarapid mutation detection by multiplex, solid-phase chemical cleavage.

P. Green, S. Saad, F. Giannelli, 1995, Genomics.

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)

A. Morris, K. Ayres, F. Giannelli, 2003, Journal of thrombosis and haemostasis : JTH.

Two factor IX mutations in the family of an isolated haemophilia B patient: direct carrier diagnosis by amplification mismatch detection (AMD)

D. Bentley, P. Green, R. Ljung, 1990, Human Genetics.

A new strategy for the genetic counselling of diseases of marked mutational heterogeneity: haemophilia B as a model.

D. Bentley, P. Green, S. Saad, 1992, Journal of medical genetics.

A new strategy for carrier and prenatal diagnosis and molecular studies in haemophilia B.

D. Bentley, R. Ljung, I. Nilsson, 1991, Current studies in hematology and blood transfusion.

Mutation analysis and genetic service: the construction and use of national confidential databases of mutations and pedigrees.

F. Giannelli, P. Green, N. Waseem, 1997, Genetic testing.

Analysis of the haemophilia A mutation in sporadic patients registered at the Royal London Hospital and their families

P. Green, B. Colvin, F. Giannelli, 1997, Haemophilia : the official journal of the World Federation of Hemophilia.

Beta-hexosaminidase splice site mutation has a high frequency among non-Jewish Tay-Sachs disease carriers from the British Isles.

M. Bobrow, P. Green, P. Green, 1992, Journal of medical genetics.

Unusual expression of the F9 gene in peripheral lymphocytes hinders investigation of F9 mRNA in hemophilia B patients.

F. Giannelli, P. Green, G. Rowley, 2003, Journal of thrombosis and haemostasis : JTH.

Mutation detection by fluorescent chemical cleavage: application to hemophilia B.

D. Bentley, F. Giannelli, P. Green, 1994, PCR methods and applications.

Haemophilia B: database of point mutations and short additions and deletions--fourth edition, 1993

M. Goossens, F. Giannelli, P. M. Green, 1993, Nucleic Acids Res..