Philippe de Mazancourt

6PUBLICATIONS
8CO-AUTHORS
HaematologyMedical molecular engineering of nucleic acids and proteinsGene expression (incl. microarray and other genome-wide approaches)NeurogeneticsMedical infection agents (incl. prions)
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Publications (6)

|Jan 10, 2026
A Simple Restriction Fragment Length Polymorphism-Based Method for Multiplex Testing of Thrombosis Risk Factors FV Leiden and F2 G20210A with Highly Sensitive Contamination Detection.

Philippe de Mazancourt, Sylvie Grey, Elise Alabre

|Dec 09, 2023
Absence of Missense Variant Detection in Inherited Dysfibrinogenemia May Result from a Poor Raw Data Analysis Algorithm or Mosaicism.

Philippe De Mazancourt, Elisabeth Mazoyer, Myriam Hormi

|May 30, 2023
A focus on dominant negative variants in a series of 170 heterozygous FXI-deficient patients.

Philippe de Mazancourt, Florence Quélin, Claire Flaujac

|Oct 04, 2022
Reinvestigation of unidentified causative variants in FXI-deficient patients: Focus on gene segment deletions.

Philippe De Mazancourt, Annie Harroche, Katia Pouymayou

|Apr 30, 2022
Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria.

Soraya Hadjali-Saichi, Philippe de Mazancourt, Jacqueline Tapon-Bretaudière

|Jan 18, 2021
A Simple RFLP-Based Method for HFE Gene Multiplex Amplification and Determination of Hereditary Hemochromatosis-Causing Mutation C282Y and H63D Variant with Highly Sensitive Determination of Contamination.

Ludmilla Ogouma-Aworet, Jean-Pierre Rabes, Philippe de Mazancourt

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Frequent Collaborators

2 joint publications

Jean-Pierre Rabes

1 joint publications

Ludmilla Ogouma-Aworet

1 joint publications

Annie Harroche

1 joint publications

Brigitte Tardy