A. Montandon

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.

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

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

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

S. Saad, F. Giannelli, A. Montandon, 2022 .

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.

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.

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.

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.

Haplotype Analysis of Identical Factor IX Mutants Using PCR

R. Ljung, F. Giannelli, A. Montandon, 1992, Thrombosis and Haemostasis.

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.

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.