Philippe De Mazancourt (Philippe de Mazancourt)

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 5

Top Topics

Quality Control

Top Venues

Haemophilia : the official journal of the World Federation of Hemophilia

BioMed research international

International journal of molecular sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Philippe De Mazancourt, Elisabeth Mazoyer, Myriam Hormi, Michel Hanss
Absence of Missense Variant Detection in Inherited Dysfibrinogenemia May Result from a Poor Raw Data Analysis Algorithm or Mosaicism. International journal of molecular sciences 24 (23) (2023)
Philippe De Mazancourt, Florence Quélin, Claire Flaujac, Emmanuelle de Raucourt, Philippe Gautier, Frédéric Bauduer, Vincent Ernest, Philippe Beurrier, Aurélie Avril, Roseline d'Oiron, Christine Biron-Andréani, Sandrine Meunier, Yesim Dargaud
A focus on dominant negative variants in a series of 170 heterozygous FXI-deficient patients. Haemophilia : the official journal of the World Federation of Hemophilia (2023)
Soraya Hadjali-Saichi, Philippe De Mazancourt, Jacqueline Tapon-Bretaudière, Tristan Mirault, Kahina Guenounou, Issam Frigaa, Anne-Marie Fischer, Ouerdia Chafa, Dominique Helley
Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria. Haemophilia : the official journal of the World Federation of Hemophilia 28 (5) (2022)
Philippe De Mazancourt, Annie Harroche, Katia Pouymayou, Marianne Sigaud, Céline Falaise, Natalie Stieltjes, Sabine-Marie Castet, Brigitte Tardy, Christophe Zawadzki, Jenny Goudemand, Yesim Dargaud
Reinvestigation of unidentified causative variants in FXI-deficient patients: Focus on gene segment deletions. Haemophilia : the official journal of the World Federation of Hemophilia (2022)
Ludmilla Ogouma-Aworet, Jean-Pierre Rabes, Philippe De Mazancourt
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. BioMed research international 2020 (2020)